Alternatived Products of [ 621-07-8 ]
Product Details of [ 621-07-8 ]
CAS No. : | 621-07-8 |
MDL No. : | MFCD00004772 |
Formula : |
C14H15NO
|
Boiling Point : |
- |
Linear Structure Formula : | - |
InChI Key : | GXELTROTKVKZBQ-UHFFFAOYSA-N |
M.W : |
213.28
|
Pubchem ID : | 69297 |
Synonyms : |
|
Application In Synthesis of [ 621-07-8 ]
* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.
- Downstream synthetic route of [ 621-07-8 ]
- 1
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[ 60-29-7 ]
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[ 52742-32-2 ]
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[ 141-52-6 ]
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[ 621-07-8 ]
- 2
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[ 64-17-5 ]
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[ 52742-32-2 ]
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[ 93-89-0 ]
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[ 621-07-8 ]
- 3
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[ 3376-26-9 ]
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[ 621-07-8 ]
Reference:
[1]Tetrahedron Letters,2002,vol. 43,p. 4369 - 4371
[2]Collection of Czechoslovak Chemical Communications,1955,vol. 20,p. 202,207
[3]Tetrahedron,1973,vol. 29,p. 4189 - 4193
- 4
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[ 932-90-1 ]
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[ 621-07-8 ]
- 5
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[ 302-17-0 ]
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[ 621-07-8 ]
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[ 3307-65-1 ]
- 6
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[ 20893-01-0 ]
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[ 621-07-8 ]
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C24H22N4O4S
[ No CAS ]
- 7
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[ 541-59-3 ]
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[ 621-07-8 ]
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[ 111363-55-4 ]
- 8
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[ 930-88-1 ]
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[ 621-07-8 ]
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[ 111363-54-3 ]
- 9
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[ 941-69-5 ]
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[ 621-07-8 ]
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[ 111363-47-4 ]
- 10
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[ 1631-25-0 ]
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[ 621-07-8 ]
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[ 111363-51-0 ]
- 11
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[ 13118-04-2 ]
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[ 621-07-8 ]
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[ 111363-50-9 ]
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[ 111363-49-6 ]
- 12
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[ 3006-93-7 ]
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[ 621-07-8 ]
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[ 117022-12-5 ]
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[ 117022-11-4 ]
- 13
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[ 52742-32-2 ]
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[ 621-07-8 ]
- 14
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[ 13676-54-5 ]
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[ 621-07-8 ]
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[ 111363-52-1 ]
- 15
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[ 28539-14-2 ]
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phenylmagnesium bromide
[ No CAS ]
-
[ 621-07-8 ]
- 16
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[ 100-39-0 ]
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[ 622-33-3 ]
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[ 622-30-0 ]
-
[ 621-07-8 ]
- 17
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[ 403-43-0 ]
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[ 621-07-8 ]
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[ 136834-98-5 ]
- 18
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[ 329-15-7 ]
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[ 621-07-8 ]
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[ 136834-99-6 ]
- 19
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[ 17450-30-5 ]
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[ 621-07-8 ]
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[ 111363-48-5 ]
- 20
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[ 100-07-2 ]
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[ 621-07-8 ]
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[ 60319-57-5 ]
- 21
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[ 4231-35-0 ]
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[ 621-07-8 ]
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[ 1114-51-8 ]
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[ 100-52-7 ]
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[ 100-46-9 ]
- 22
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[ 103-49-1 ]
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[ 77681-22-2 ]
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[ 621-07-8 ]
- 23
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[ 103-49-1 ]
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[ 77681-22-2 ]
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[ 100-52-7 ]
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[ 27845-50-7 ]
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[ 621-07-8 ]
- 24
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[ 621-07-8 ]
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[ 77681-22-2 ]
- 25
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[ 88-67-5 ]
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[ 621-07-8 ]
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O-2-iodobenzoyl-N,N-dibenzylhydroxylamine
[ No CAS ]
- 26
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[ 621-07-8 ]
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[ 2631-23-4 ]
- 27
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[ 621-07-8 ]
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[ 67723-10-8 ]
- 28
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[ 621-07-8 ]
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[ 197717-82-1 ]
- 29
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[ 103-49-1 ]
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aqueous dioxane
[ No CAS ]
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[ 621-07-8 ]
- 30
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[ 2525-62-4 ]
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[ 621-07-8 ]
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[ 113659-05-5 ]
Yield | Reaction Conditions | Operation in experiment |
7.5 g (88%) |
|
EXAMPLE 8 N-n-Hexyl-O-(N,N-dibenzylamino)carbamate The procedure of Example 1 is repeated using 5.33 g (25 mmol) of <strong>[621-07-8]N,N-dibenzylhydroxylamine</strong> and 3.18 g (25 mmol) of n-hexyl isocyanate. The residue is recrystallized from heptane to give 7.5 g (88%) of a white solid, m.p. 72-73.5 C. Anal. Calcd. for C21 H28 N2 O2: C, 74.1; H, 8.3; N, 8.2. Found: C, 74.4; H, 8.2; N, 8.2. |
- 31
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[ 111-36-4 ]
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[ 621-07-8 ]
-
[ 113659-10-2 ]
Yield | Reaction Conditions | Operation in experiment |
6.8 g (87%) |
In tetrahydrofuran; |
EXAMPLE 1 N-Butyl-O-(N-N-dibenzylamino)carbamate A solution of 5.33 g (25 mmol) of <strong>[621-07-8]N,N-dibenzylhydroxylamine</strong> in 25 ml of dry tetrahydrofuran is admixed with 2.48 g (25 mmol) of n-butyl isocyanate and the mixture is stirred for four hours. The solvent is removed in vacuo and the residue is recrystallized from heptane to give 6.8 g (87%) of a white solid, m.p 81-82 C. Anal. Calcd. for C19 H24 N2 O2: C, 73.0; H, 7.7; N, 9.0. Found: C, 73.0; H, 7.7; N, 8.8. |
- 32
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[ 821-06-7 ]
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[ 621-07-8 ]
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[ 137359-64-9 ]
Yield | Reaction Conditions | Operation in experiment |
|
In tetrahydrofuran; water; |
EXAMPLE 6 O,O'-But-2-en-1,4-diyl-bis(<strong>[621-07-8]N,N-dibenzylhydroxylamine</strong>) In a 1000 ml three-necked flash fitted with a thermometer, an addition funnel and a condenser topped with a nitrogen sweep is charged 6.0 g (120 mmol) of a 50% oil dispersion of sodium hydride. The sodium hydride is washed twice with 20 ml-portions of pentane to remove the oil. The sodium hydride is then suspended in 100 ml of tetrahydrofuran. Into the resultant suspension, which is now cooled to -5 C., is added dropwise a solution of 25.0 g (120 mmol) of <strong>[621-07-8]N,N-dibenzylhydroxylamine</strong> in 150 ml of tetrahydrofuran. After the addition is complete, the reaction mixture is heated under reflux at 50 to 60 C. till gas (hydrogen) evolution ceases (this takes approximately six hours). The reaction mixture is then cooled in an ice water bath and a solution of 12.8 g (60 mmol) of 1,4-dibromo-2-butene in 60 ml of tetrahydrofuran is added to the reaction mixture maintaining the reaction temperature at about 5 C. during the addition step. After the addition is complete, the reaction mixture is heated under reflux at 50-60 C. for six hours. The cooled reaction mixture is then treated with 100 ml of water. The resultant layers are separated and the organic layer is dried over anhydrous magnesium sulfate. Evaporation of the solvent gives 24.5 g of a crude yellow solid residue. A 15.0 g-portion of said residue is purified by HPLC (silica gel, 95:5 v/v hexane:ethyl acetate eluent) to give 1.42 g of a viscous yellow oil which was crystallized from hexane to give 0.87 g of the title compound as a white solid melting at 82-85 C. Analysis: Calcd for C32 H34 N2 O2: C, 80.3; H, 7.2; N, 5.9. Found: C, 80.3; H, 7.2; N, 5.6. |
- 33
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[ 822-06-0 ]
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[ 621-07-8 ]
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[ 113659-07-7 ]
Yield | Reaction Conditions | Operation in experiment |
6.6 g (89%) |
|
EXAMPLE 4 N,N'-(1,6-Hexanediyl)-bis[O-(N,N-dibenzylamino)carbamate] The procedure of Example 1 is repeated using 5.33 g (25 mmol) of <strong>[621-07-8]N,N-dibenzylhydroxylamine</strong> and 2.10 g (1.25 mmol) of 1,6-hexanediisocyanate. The residue is recrystallized from 2-propanol to give 6.6 g (89%) of a white solid, m.p. 121-124 C. Anal. Calcd. for C36 H42 N4 O4: C, 72.7; H, 7.1; N, 9.3. Found: C, 72.6; H, 7.1; N, 9.4. |
- 34
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[ 4098-71-9 ]
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[ 621-07-8 ]
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[ 113659-04-4 ]
Yield | Reaction Conditions | Operation in experiment |
11.0 g (68%) |
|
EXAMPLE 9 1-{N-[O-(N,N-dibenzylamino)carboxy]amino}-3-{N-[O-(N,N-dibenzylamino)carboxy]amino}methyl-3,5,5-trimethylcyclohexane. The procedure of Example 1 is repeated using 10.66 g (50 mmol) of <strong>[621-07-8]N,N-dibenzylhydroxylamine</strong> and 5.56 g (25 mmole) of 3-isocyanatomethyl-3,5,5-trimethylcyclohexylisocyanate. The residue is recrystallized from a 1:1 heptane: toluene solvent mixture to give 11.0 g (68%) of a white soldi, m.p. 139-146 C. Anal. Calcd. for C40 H48 N4 O4: C, 74.0; H, 7.5; N, 8.6. Found: C, 74.0; H, 7.7; N, 8.7. |
- 35
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[ 621-07-8 ]
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N,N-Dibenzyl-O-carbamylhydroxylamine
[ No CAS ]
Yield | Reaction Conditions | Operation in experiment |
|
With hydrogenchloride; In methanol; water; |
EXAMPLE 7 N,N-Dibenzyl-O-carbamylhydroxylamine A stirred suspension of 10.70 g of <strong>[621-07-8]N,N-dibenzylhydroxylamine</strong> in 25 ml of methanol is admixed dropwise with a solution of 4.53 ml conc. hydrochloric acid in 10 ml of water. A solution of 4.06 g of potassium cyanate in 15 ml of water is then added and the resulting suspension is stirred at room temperature for 3 hours. The crude product is removed by filtration and further purified by liquid chromatography to afford the title compound as a white solid; m.p. 127-29 C. Anal. Calcd. for C15 H16 N2 O2: C, 70.3; H, 6.3; N, 10.9. Found: C, 70.2; H, 6.3; N, 11.2. |
- 36
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[ 865-47-4 ]
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[ 292638-85-8 ]
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[ 621-07-8 ]
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methyl 3-[N,N-dibenzylaminoxy]propanoate
[ No CAS ]
Yield | Reaction Conditions | Operation in experiment |
|
In tetrahydrofuran; |
EXAMPLE I Methyl-3-[N,N-dibenzylaminoxy]propanoate A solution of 42.6 g of <strong>[621-07-8]N,N-dibenzylhydroxylamine</strong>, 25.8 g of methyl acrylate and 2.0 g of potassium-tert-butoxide in 200 ml of tetrahydrofuran is heated under reflux for 12 hours under N2. The crude reaction mixture is concentrated under reduced pressure and the residue is partitioned between water and ether. The orcanic layer is washed with water, saturated NaHSO4 solution and brine, dried (MgSO4) and then evaporated under reduced pressure to give the title compound as an oil. Anal. calcd. for C18 H21 NO3: C, 72.2; H, 7.1; N, 4.7. Found: C, 72.2; H, 7.1; N, 4.7. |
- 37
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[ 865-47-4 ]
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[ 292638-85-8 ]
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[ 621-07-8 ]
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[ 110878-50-7 ]
Yield | Reaction Conditions | Operation in experiment |
|
In ethanol; |
EXAMPLE II Ethyl-3-[N,N-dibenzylaminoxy]propanoate The procedure of Example I is repeated using 21.33 g of <strong>[621-07-8]N,N-dibenzylhydroxylamine</strong>, 10.33 g of methyl acrylate and 1.0 g of potassium-tert-butoxide in 100 ml of ethanol, to afford the title compound as a colorless liquid. Anal. calcd. for C19 H23 NO3: C, 72.8; H, 7.4; N, 4.5. Found: C, 72.4; H, 7.5; N, 4.4. |
- 38
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[ 107-58-4 ]
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[ 865-47-4 ]
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[ 621-07-8 ]
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[ 112915-25-0 ]
Yield | Reaction Conditions | Operation in experiment |
|
In tetrahydrofuran; |
EXAMPLE I N-tert-butyl-[3-(N,N-dibenzylaminoxy)-propionamide] A solution of 21.33 g of dibenzylhydroxylamine in 100 ml of dry tetrahydrofuran is admixed with 1.12 g of potassium-tert-butoxide followed by 12.70 g of N-tert-butylacrylamide. The solution is heated under reflux for 24 hours under N2. The crude reaction mixture is concentrated under reduced pressure and the residue is partitioned between water and methylene chloride. The organic layer is washed with water, brine dried (MgSO4) and evaporated under reduced pressure. Purification by liquid chromatography affords the title compound as an oil. Anal. calcd. for C21 H28 N2 O2: C, 74.1; H, 8.3; N, 8.2. Found: C, 74.3; H, 8.5; N, 8.3. |
- 39
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[ 4813-57-4 ]
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[ 865-47-4 ]
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[ 621-07-8 ]
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[ 110878-53-0 ]
Yield | Reaction Conditions | Operation in experiment |
|
In tetrahydrofuran; |
EXAMPLE V Octadecyl-3-[N,N-dibenzylaminoxy]propanoate The procedure of Example I is repeated using 10.66 g of <strong>[621-07-8]N,N-dibenzylhydroxylamine</strong>, 16.03 g of n-octadecyl acrylate, and 0.50 g of potassium-tert-butoxide in 100 ml of tetrahydrofuran, to afford the title compound as a colorless oil. Anal. calcd. for C35 H55 NO3: C, 78.2; H, 10.3; N, 2.6. Found: C, 78.0; H, 10.2; N, 2.6. |
- 40
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[ 105-75-9 ]
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[ 865-47-4 ]
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[ 621-07-8 ]
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[ 110878-61-0 ]
Yield | Reaction Conditions | Operation in experiment |
|
In tetrahydrofuran; |
EXAMPLE I Di-n-butyl-2-(N,N-dibenzylaminoxy)succinate A solution of 10.0 g of <strong>[621-07-8]N,N-dibenzylhydroxylamine</strong>, 10.7 g of di-n-butylmaleate and 0.53 g of potassium-tert-butoxide in 100 ml of tetrahydrofuran is heated under reflux for 48 hours. The crude reaction mixture is concentrated under reduced pressure and the residue is partitioned between water and methylene chloride. The organic layer is washed with water, brine, dried (MgSO4) and then evaporated under reduced pressure. Purification by liquid chromatography affords the title compound as a colorless oil. Anal. Calcd. for C26 H35 NO5: C, 70.7; H, 8.0; N, 3.2. Found: C, 70.5; H, 8.2; N, 3.0. |
- 41
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[ 142-16-5 ]
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[ 621-07-8 ]
-
[ 110878-62-1 ]
Yield | Reaction Conditions | Operation in experiment |
|
In tetrahydrofuran; |
EXAMPLE II Di-2-ethylhexyl-2-(N,N-dibenzylaminoxy)succinate A solution of 13.67 g of <strong>[621-07-8]N,N-dibenzylhydroxylamine</strong> and 21.82 g of di-(2-ethylhexyl)maleate in 50 ml of tetrahydrofuran is heated under reflux for 48 hours. The solvent is removed under reduced pressure and the residue is chromatographed to afford the title compound as a clear colorless liquid. Anal. Calcd. for C34 H51 NO5: C, 73.7; H, 9.3; N, 2.5. Found: C, 72.6; H, 9.3; N, 2.2. |
- 42
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3-(3,5-di-tert-butyl-4-hydroxybenzylthio)propanoic acid
[ No CAS ]
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[ 79-37-8 ]
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[ 621-07-8 ]
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[ 123173-43-3 ]
Yield | Reaction Conditions | Operation in experiment |
|
With triethylamine; |
EXAMPLE IV O-(3,5-Di-tert.butyl-4-hydroxybenzylthio)propionyl-N,N-dibenzylhydroxylamin The compound is prepared using the method of Example II, with 16.20 g of 3-(3,5-di-tert-butyl-4-hydroxybenzylthio)propanoic acid, 10.66 g of <strong>[621-07-8]N,N-dibenzylhydroxylamine</strong>, 5.06 g of triethylamine, and 6.35 g of oxalyl chloride. The residue is purified by preparative HPLC to give 3.0 g of a white solid: mp 84-86 C. Anal. Calcd. for C32 H41 NO3 S: C, 74.0; H, 8.0; N, 2.7. Found: C, 73.8; H, 8.0; N, 2.6. |
- 43
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[ 40056-43-7 ]
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[ 621-07-8 ]
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O-(3,5-Di-tert-butyl-4-hydroxybenzoyl)-N,N-dibenzylhydroxylamine
[ No CAS ]
Yield | Reaction Conditions | Operation in experiment |
|
With pyridine; In dichloromethane; |
EXAMPLE I O-(3,5-Di-tert-butyl-4-hydroxybenzoyl)-<strong>[621-07-8]N,N-dibenzylhydroxylamine</strong> To a solution of 27.9 g of dibenzylhydroxylamine and 10.3 gof pyridine in 100 ml of methylene chloride is added a solution of 39.0 g of 3,5-di-tert-butyl-4-hydroxybenzoyl chloride in 100 ml of methylene chloride. After stirring the mixture at room temperature for 24 hours, the reaction mixture is washed with 10% aqueous hydrochloric acid, water, brine and dried. Evaporation followed by crystallization of the residue from heptane affords the title compound as a white solid: mp 90-92 C. Anal. Calcd. for C29 H35 NO3: C, 78.2; H, 7.9; N, 3.1. Found: C, 78.8; H, 8.0; N, 3.2. |
- 44
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bis(acetylacetonato)dioxidomolybdenum(VI)
[ No CAS ]
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[ 621-07-8 ]
-
[ 74081-87-1 ]
- 45
-
[ 13520-76-8 ]
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[ 621-07-8 ]
-
[ 99491-82-4 ]
- 46
-
[ 788133-24-4 ]
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[ 621-07-8 ]
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((C2H5)2NO)2OVOVO(ON(C2H5)2)2
[ No CAS ]
- 47
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[ 546-68-9 ]
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[ 621-07-8 ]
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[ 83678-81-3 ]
- 48
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ammonium vanadate(V)
[ No CAS ]
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[ 621-07-8 ]
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((C2H5)2NO)2OVOVO(ON(C2H5)2)2
[ No CAS ]
- 49
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[ 546-68-9 ]
-
[ 2217-15-4 ]
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[ 621-07-8 ]
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Ti2(OCH(CO2CH(CH3)2)CHO(CO2CH(CH3)2))3(ON(CH2C6H5)2)2
[ No CAS ]
- 50
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ammonium vanadate(V)
[ No CAS ]
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[ 621-07-8 ]
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{(VO(ON(C6H5CH2)2)2)2O}
[ No CAS ]
- 51
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Pd2(CH3COO)C6H2(CH3)(S)(CHNNC(O)C6H11)2
[ No CAS ]
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[ 621-07-8 ]
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(C23H29N4O2S)Pd2((C6H5CH2)2NO)
[ No CAS ]
- 52
-
[ 143645-67-4 ]
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[ 621-07-8 ]
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[ 245414-27-1 ]
- 53
-
[ 342028-87-9 ]
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[ 621-07-8 ]
-
[ 851474-63-0 ]
- 54
-
[ 330476-12-5 ]
-
[ 621-07-8 ]
-
[ 851474-70-9 ]
- 55
-
[ 330476-14-7 ]
-
[ 621-07-8 ]
-
[ 851474-58-3 ]
- 56
-
[ 17520-19-3 ]
-
[ 621-07-8 ]
-
[ 677796-55-3 ]
- 57
-
[ 15617-14-8 ]
-
[ 28005-97-2 ]
-
[ 621-07-8 ]
-
[ 851514-46-0 ]
-
[ 851514-46-0 ]
- 58
-
[ 28005-97-2 ]
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[ 621-07-8 ]
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[ 851514-46-0 ]
- 59
-
[ 16853-53-5 ]
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[ 621-07-8 ]
-
[ 926895-70-7 ]
- 60
-
[ 621-07-8 ]
-
[ 20438-95-3 ]
Yield | Reaction Conditions | Operation in experiment |
68% |
With hydrogenchloride; In n-heptane; isopropyl alcohol; at 20℃; |
Example 1 (10.7 g, 0.05 mole) is dissolved in 35 mL of heptane and 35 mL of anhydrous isopropanol. To this stirred solution is added dropwise 9. 38 g of absolute isopropanol containing 0.05 mole of hydrochloric acid at ambient temperature. The resulting white precipitate is filtered, recrystallized from 400 g of boiling isopropanol, and dried to constant weight in a vacuum oven. The title compound is received (8. 5 g, 68 % yield) as a white solid with a melting point of 174C whose structure is consistent with HNMR. |
- 61
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tris{bis(dimethylsilyl)amido}bis(tetrahydrofuran)yttrium
[ No CAS ]
-
[ 621-07-8 ]
-
[ 1104626-53-0 ]
- 62
-
[ 103-49-1 ]
-
[ 3376-26-9 ]
-
[ 100-52-7 ]
-
[ 621-07-8 ]
- 63
-
[ 103-49-1 ]
-
[ 780-25-6 ]
-
[ 100-52-7 ]
-
[ 621-07-8 ]
- 64
-
[ 937-14-4 ]
-
[ 212203-90-2 ]
-
(RS)-N,N-dibenzyl-O-cyclohexen-3-yl-hydroxylamine
[ No CAS ]
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C7H5ClO2*C20H23NO
[ No CAS ]
-
[ 621-07-8 ]
- 65
-
[ 188724-74-5 ]
-
[ 621-07-8 ]
-
[ 1273536-14-3 ]
- 66
-
[ 330476-12-5 ]
-
[ 621-07-8 ]
-
[ 851474-58-3 ]
- 67
-
tris(cyclopentadienyl)yttrium
[ No CAS ]
-
[ 621-07-8 ]
-
[Cp2Y(N,N-dibenzylhydroxylamino)]2
[ No CAS ]
- 68
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tris(cyclopentadienyl)samarium
[ No CAS ]
-
[ 621-07-8 ]
-
[Cp2Sm(N,N-dibenzylhydroxylamino)]2
[ No CAS ]
- 69
-
[ 123-72-8 ]
-
[ 536-74-3 ]
-
[ 621-07-8 ]
-
[ 1145680-23-4 ]
Yield | Reaction Conditions | Operation in experiment |
58% |
With copper(I) bromide; In toluene; at 70℃; for 24h;Inert atmosphere; |
General procedure: To a 25-mL flask equipped with a magnetic stirrer, in which the air was replaced by N2, was added CuBr (0.05 mmol), toluene (1.0 mL), aldehyde (1.0 mmol), alkyne (1.5 mmol), and hydroxylamine (1.5 mmol). The mixture was stirred at 70C. After the completion of the reaction (monitored by TLC), the reaction solution was submitted to flash chromatographic separation on silica gel using petroleum ether/ethyl acetate as an eluent to give the corresponding product. |
- 70
-
[ 123-72-8 ]
-
[ 536-74-3 ]
-
[ 621-07-8 ]
-
[ 1145680-23-4 ]
-
[ 3376-26-9 ]
Yield | Reaction Conditions | Operation in experiment |
19%; 33% |
With copper(I) bromide; In toluene; at 70℃; for 0.5h;Inert atmosphere; |
General procedure: To a 25-mL flask equipped with a magnetic stirrer, in which the air was replaced by N2, was added CuBr (0.05 mmol), toluene (1.0 mL), aldehyde (1.0 mmol), alkyne (1.5 mmol), and hydroxylamine (1.5 mmol). The mixture was stirred at 70C. After the completion of the reaction (monitored by TLC), the reaction solution was submitted to flash chromatographic separation on silica gel using petroleum ether/ethyl acetate as an eluent to give the corresponding product. |
- 71
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[ 1467-79-4 ]
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[ 621-07-8 ]
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[ 1450882-11-7 ]
- 72
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[ 100-47-0 ]
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[ 621-07-8 ]
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[ 1450882-12-8 ]
- 73
-
[ 140-29-4 ]
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[ 621-07-8 ]
-
[ 1450882-13-9 ]
- 74
-
[ 617-83-4 ]
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[ 621-07-8 ]
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[ 1450882-14-0 ]
- 75
-
[ 1530-87-6 ]
-
[ 621-07-8 ]
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[ 1450882-15-1 ]
- 76
-
[ 1530-89-8 ]
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[ 621-07-8 ]
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[ 1450882-16-2 ]
- 77
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[ 1450881-88-5 ]
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[ 621-07-8 ]
-
[ 1450881-98-7 ]
- 78
-
[ 1450881-90-9 ]
-
[ 621-07-8 ]
-
[ 1450882-00-4 ]
- 79
-
[ 1450881-92-1 ]
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[ 621-07-8 ]
-
[ 1450882-02-6 ]
- 80
-
[ 1450881-94-3 ]
-
[ 621-07-8 ]
-
[ 1450882-04-8 ]
- 81
-
[ 887144-97-0 ]
-
[ 621-07-8 ]
-
N,N-dibenzyl-O-trifluoromethylhydroxylamine
[ No CAS ]
- 82
-
[ 887144-97-0 ]
-
[ 2564-83-2 ]
-
[ 621-07-8 ]
-
[ 1335135-19-7 ]
-
N,N-dibenzyl-O-trifluoromethylhydroxylamine
[ No CAS ]
- 83
-
[ 887144-97-0 ]
-
[ 2564-83-2 ]
-
[ 621-07-8 ]
-
[ 1335135-19-7 ]
- 84
-
[ 137768-73-1 ]
-
[ 621-07-8 ]
-
[ 1623815-61-1 ]
-
[ 1623815-75-7 ]
- 85
-
[ 137768-73-1 ]
-
[ 621-07-8 ]
-
[ 1623815-75-7 ]