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[ CAS No. 114873-52-8 ] {[proInfo.proName]}

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Chemical Structure| 114873-52-8
Chemical Structure| 114873-52-8
Structure of 114873-52-8 * Storage: {[proInfo.prStorage]}
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Product Details of [ 114873-52-8 ]

CAS No. :114873-52-8 MDL No. :MFCD09263320
Formula : C20H38N4O6 Boiling Point : -
Linear Structure Formula :- InChI Key :BPEUICGMDOXPJJ-UHFFFAOYSA-N
M.W : 430.54 Pubchem ID :10906130
Synonyms :

Safety of [ 114873-52-8 ]

Signal Word:Warning Class:
Precautionary Statements:P264-P280-P302+P352+P332+P313+P362+P364-P305+P351+P338+P337+P313 UN#:
Hazard Statements:H315-H319 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 114873-52-8 ]

* 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 [ 114873-52-8 ]

[ 114873-52-8 ] Synthesis Path-Downstream   1~46

  • 1
  • [ 105-36-2 ]
  • [ 294-90-6 ]
  • [ 114873-52-8 ]
  • tetraethyl 2,2',2'',2'''-(1,4,7,10-tetraazacyclododecane-1,4,7,10-tetrayl)tetraacetate [ No CAS ]
  • 2
  • [ 100-11-8 ]
  • [ 114873-52-8 ]
  • [4,7-Bis-ethoxycarbonylmethyl-10-(4-nitro-benzyl)-1,4,7,10-tetraaza-cyclododec-1-yl]-acetic acid ethyl ester [ No CAS ]
  • 4
  • [ 114873-52-8 ]
  • [ 5437-45-6 ]
  • (4,7,10-Tris-ethoxycarbonylmethyl-1,4,7,10-tetraaza-cyclododec-1-yl)-acetic acid benzyl ester [ No CAS ]
  • 5
  • [ 105-36-2 ]
  • [ 294-90-6 ]
  • [ 114873-52-8 ]
  • [ 468743-81-9 ]
  • 6
  • [ 574-98-1 ]
  • [ 114873-52-8 ]
  • [ 1026728-56-2 ]
  • 7
  • [ 866925-25-9 ]
  • [ 114873-52-8 ]
  • [ 866925-27-1 ]
  • 8
  • [ 114873-52-8 ]
  • [7-(2-Amino-ethyl)-4,10-bis-ethoxycarbonylmethyl-1,4,7,10-tetraaza-cyclododec-1-yl]-acetic acid ethyl ester [ No CAS ]
  • 9
  • [ 114873-52-8 ]
  • 10-(2-aminoethyl)-1,4,7,10-tetraazacyclododecane-1,4,7-tris(methylcarboxylic acid) [ No CAS ]
  • 10
  • [ 114873-52-8 ]
  • [ 114873-54-0 ]
  • 11
  • [ 114873-52-8 ]
  • [4-({2-[2-(2-Benzyloxycarbonylamino-ethoxy)-ethoxy]-ethylcarbamoyl}-methyl)-7,10-bis-ethoxycarbonylmethyl-1,4,7,10-tetraaza-cyclododec-1-yl]-acetic acid ethyl ester [ No CAS ]
  • 12
  • [ 114873-52-8 ]
  • [4-({2-[2-(2-Amino-ethoxy)-ethoxy]-ethylcarbamoyl}-methyl)-7,10-bis-ethoxycarbonylmethyl-1,4,7,10-tetraaza-cyclododec-1-yl]-acetic acid ethyl ester; hydrochloride [ No CAS ]
  • 13
  • [ 114873-52-8 ]
  • (4,7-bis-carboxymethyl-10-[2-(2-{2-[21-(2-mercapto-ethylcarbamoyl)-heneicosa-10,12-diynoylamino]-ethoxy}-ethoxy)-ethylcarbamoyl]-methyl}-1,4,7,10tetraaza-cyclododec-1-yl)-acetic acid [ No CAS ]
  • 14
  • [ 114873-52-8 ]
  • (4-[2-(2-{2-[21-(2-acetylsulfanyl-ethylcarbamoyl)-heneicosa-10,12-diynoylamino]-ethoxy}-ethoxy)-ethylcarbamoyl]-methyl}-7,10-bis-ethoxycarbonylmethyl-1,4,7,10tetraaza-cyclododec-1-yl)-acetic acid ethyl ester [ No CAS ]
  • 15
  • [ 114873-52-8 ]
  • [ 149440-35-7 ]
  • 16
  • Diethyl phosphonate [ No CAS ]
  • [ 122-51-0 ]
  • [ 114873-52-8 ]
  • [ 885511-60-4 ]
  • [ 64-17-5 ]
YieldReaction ConditionsOperation in experiment
80% at 140℃; for 1.5h; Example 45; Preparation of heptaethyl ester 10-fbisfohosphono)methyl]-1.4.7,10- tetraazacvclododecane-1,4,7-triacetic (Et7DO3AP2) and lO-Fbisfphosphono) methvn-1 ,4.7.10-tetraazacvclododecane-1.4.7-triacetic (DQ3AP2) via triethyl ester 1 ,4,7,10-tetraazacvclododecane-1.4.7-triacetic acid (EtaDQ3A); a) A mixture of Et3DO3A 22,8 g (53 mmol), triethyl orthoformate 9,3 g (63 mmol) and diethyl phosphite 29,3 g (212 mmol) was stirred at 140 0C for 1 ,5 h with continuous removal of the ethanol formed. After cooling the volatiles were removed in vacuo. The residue was chromatographed on silica gel EPO <DP n="120"/>- US - using CHCI3-MeOH-NH3 (49:1 :1) as an eluent to give 30,4 g Et7DO3AP2 as a pale yellow oil. Total yield: 80 percent.
  • 17
  • N-(2-(4-methoxyphenylethyl)-N-[(2-oxiranyl)-methyl]-methanesulfonic acid amide [ No CAS ]
  • [ 114873-52-8 ]
  • [ 170215-91-5 ]
YieldReaction ConditionsOperation in experiment
7.02 g (49.0%) In ethanol; EXAMPLE 9a 1-[3-(N-[2-(4-Methoxyphenyl)-ethyl]-mesylamino)-2-hydroxypropyl]-4,7,10-tris-(ethoxycarbonylmethyl)-1,4,7,10-tetraazacyclododecane 200 ml of absolute ethanol is poured over 8.61 g (20 mmol) of N,N',N"-tris-(ethoxycarbonylmethyl)-1,4,7,10-tetraazacyclododecane (produced according to DE 36 25 417 A1) in a bomb tube. After 5.71 g (20 mmol) of N-(2-(4-methoxyphenylethyl)-N-[(2-oxiranyl)-methyl]-methanesulfonic acid amide is added (Example 2g), the bomb tube is closed, flushed with nitrogen, and the resulting reaction mixture is heated for 16 hours to 90 C. After the reaction (TLC control) is completed, the solvent is evaporated in a vacuum and the yellowish, oily residue is chromatographed on silica gel (eluent: chloroform/methanol; methanol: 0-80%). Yield: 7.02 g (49.0%), colorless oil Analysis: Relative to the anhydrous substance Cld: C 55.36 H 8.03 N 9.78 S 4.48 O 22.35 Fnd: C 55.17 H 7.89 N 9.45 S 4.32 O
  • 18
  • N-›2-benzyloxy)-ethyl)-N-[(2-oxiranyl)-methyl]-methanesulfonic acid amide [ No CAS ]
  • [ 114873-52-8 ]
  • [ 170215-93-7 ]
YieldReaction ConditionsOperation in experiment
7.61 g (53.2%) In ethanol; EXAMPLE 10a 1-{3-[N-(2-Benzyloxy-ethyl)-mesylamino]-2-hydroxypropyl}-4,7,10-tris-(ethoxycarbonylmethyl)-1,4,7,10-tetraazacyclododecane 200 ml of absolute ethanol is poured over 8.61 g (20 mmol) of N,N',N"-tris-(ethoxycarbonylmethyl)-1,4,7,10-tetraazacyclododecane (produced according to DE 36 25 417 A1) in a bomb tube. After 5.71 g (20 mmol) of N-›2-benzyloxy)-ethyl)-N-[(2-oxiranyl)-methyl]-methanesulfonic acid amide is added (Example 2h), the bomb tube is closed, flushed with nitrogen, and the resulting reaction mixture is heated for 16 hours to 90 C. After the reaction (TLC control) is completed, the solvent is evaporated in a vacuum and the yellowish, oily residue is chromatographed on silica gel (eluent: chloroform/methanol; methanol: 0-80%). Yield: 7.61 g (53.2%), colorless oil Analysis: Relative to the anhydrous substance Cld: C 55.36 H 8.03 N 9.78 S 4.48 O 22.35 Fnd: C 55.09 H 7.78 N 9.50 S 4.19 O
  • 19
  • N-((2,2-dimethyl-1,3-dioxolan-4-yl)methyl)methanesulfonamide [ No CAS ]
  • [ 114873-52-8 ]
  • [ 170216-01-0 ]
YieldReaction ConditionsOperation in experiment
7.33 g (52.7%) In ethanol; EXAMPLE 14a 1-{3-{N-[(3,3-Dimethyl-2,4-dioxa-cyclopentyl)-methyl]-mesylamino}-2-hydroxypropyl}-4,7,10-tris-(ethoxycarbonylmethyl)-1,4,7,10-tetraazacyclododecane 200 ml of absolute ethanol is poured over 8.61 g (20 mmol) of N,N',N"-tris-(ethoxycarbonylmethyl)-1,4,7,10-tetraazacyclododecane (produced according to DE 36 25 417 A1) in a bomb tube. After 5.31 g (20 mmol) of N-[(3,3-dimethyl-2,4-dioxa-cyclopentyl)-methyl]-methanesulfonic acid amide is added (Example 21), the bomb tube is closed, flushed with nitrogen, and the resulting reaction mixture is heated for 16 hours to 90 C. After the reaction (TLC control) is completed, the solvent is evaporated in a vacuum and the yellowish, oily residue is chromatographed on silica gel (eluent: chloroform/methanol; methanol: 0-80%). Yield: 7.33 g (52.7%), colorless oil Analysis: Relative to the anhydrous substance Cld: C 51.78 H 8.26 N 10.06 S 4.61 O 25.29 Fnd: C 51.51 H 8.02 N 10.21 S 4.72 O
  • 20
  • [ 170215-64-2 ]
  • [ 114873-52-8 ]
  • [ 170215-79-9 ]
YieldReaction ConditionsOperation in experiment
7.97 g (62.5%) In ethanol; EXAMPLE 3a 1-[3-(N-Butyl-mesylamino)-2-hydroxypropyl]-4,7,10-tris-(ethoxycarbonylmethyl)-1,4,7,10-tetraazacyclododecane 200 ml of absolute ethanol is poured over 8.61 g (20 mmol) of N,N',N"-tris-(ethoxycarbonylmethyl)-1,4,7,10-tetraazacyclododecane (produced according to DE 36 25 417 A1) in a bomb tube. After 4.15 g (20 mmol) of N-butyl-N-[(2-oxiranyl)-methyl]-methanesulfonic acid amide is added (Example 2a), the bomb tube is closed, flushed with nitrogen, and the resulting reaction mixture is heated for 16 hours to 90 C. After the reaction (TLC control) is completed, the solvent is evaporated in a vacuum and the yellowish, oily residue is chromatographed on silica gel (eluent: chloroform/methanol; methanol: 0-80%). Yield: 7.97 g (62.5%), colorless oil Analysis: relative to the anhydrous substance Cld: C 52.73 H 8.69 N 10.98 S 5.03 O 22.58 Fnd: C 52.51 H 8.73 N 10.79 S 4.78 O
  • 21
  • [ 170215-65-3 ]
  • [ 114873-52-8 ]
  • [ 170215-81-3 ]
YieldReaction ConditionsOperation in experiment
7.25 g (52.2%) In ethanol; EXAMPLE 4a 1-[3-(N-Octyl-mesylamino)-2-hydroxypropyl]-4,7,10-tris-(ethoxycarbonylmethyl)-1,4,7,10-tetraazacyclododecane 200 ml of absolute ethanol is poured over 8.61 g (20 mmol) of N,N',N"-tris-(ethoxycarbonylmethyl)-1,4,7,10-tetraazacyclododecane (produced according to DE 36 25 417 A1) in a bomb tube. After 5.27 g (20 mmol) of N-octyl-N-[(2-oxiranyl)-methyl]-methanesulfonic acid amide is added (Example 2b), the bomb tube is closed, flushed with nitrogen, and the resulting reaction mixture is heated for 16 hours to 90 C. After the reaction (TLC control) is completed, the solvent is evaporated in a vacuum and the yellowish, oily residue is chromatographed on silica gel (eluent: chloroform/methanol; methanol: 0-80%). Yield: 7.25 g (52.2%), colorless oil Analysis: Relative to the anhydrous substance Cld: C 55.39 H 9.15 N 10.09 S 4.62 O 20.75 Fnd: C 55.12 H 8.93 N 9.88 S 4.37 O
  • 22
  • [ 170215-66-4 ]
  • [ 114873-52-8 ]
  • [ 170215-83-5 ]
YieldReaction ConditionsOperation in experiment
7.89 g (53.6%) In ethanol; EXAMPLE 5a 1-[3-(N-Undecyl-mesylamino)-2-hydroxypropyl]-4,7,10-tris-(ethoxycarbonylmethyl)-1,4,7,10-tetraazacyclododecane 200 ml of absolute ethanol is poured over 8.61 g (20 mmol) of N,N',N"-tris-(ethoxycarbonylmethyl)-1,4,7,10-tetraazacyclododecane (produced according to DE 36 25 417 A1) in a bomb tube. After 6.11 g (20 mmol) of N-undecyl-N-[(2-oxiranyl)-methyl]-methanesulfonic acid amide is added (Example 2c), the bomb tube is closed, flushed with nitrogen, and the resulting reaction mixture is heated for 16 hours to 90 C. After the reaction (TLC control) is completed, the solvent is evaporated in a vacuum and the yellowish, oily residue is chromatographed on silica gel (eluent: chloroform/methanol; methanol: 0-80%). Yield: 7.89 g (53.6%), colorless oil Analysis: Relative to the anhydrous substance Cld: C 57.11 H 9.45 N 9.52 S 4.36 O 19.56 Fnd: C 56.97 H 9.18 N 9.43 S 4.19 O
  • 23
  • [ 170215-67-5 ]
  • [ 114873-52-8 ]
  • [ 170215-85-7 ]
YieldReaction ConditionsOperation in experiment
7.35 g (57.4%) In ethanol; EXAMPLE 6a 1-[3-(N-2-Methoxyethyl-mesylamino)-2-hydroxypropyl]-4,7,10-tris-(ethoxycarbonylmethyl)-1,4,7,10-tetraazacyclododecane 200 ml of absolute ethanol is poured over 8.61 g (20 mmol) of N,N',N"-tris-(ethoxycarbonylmethyl)-1,4,7,10-tetraazacyclododecane (produced according to DE 36 25 417 A1) in a bomb tube. After 4.19 g (20 mmol) of N-(2-methoxyethyl)-N-[(2-oxiranyl)-methyl]-methanesulfonic acid amide is added (Example 2d), the bomb tube is closed, flushed with nitrogen, and the resulting reaction mixture is heated for 16 hours to 90 C. After the reaction (TLC control) is completed, the solvent is evaporated in a vacuum, and the yellowish, oily residue is chromatographed on silica gel (eluent: chloroform/methanol; methanol: 0-80%). Yield: 7.35 g (57.4%), colorless oil Analysis: Relative to the anhydrous substance Cld: C 50.69 H 8.35 N 10.95 S 5.01 O 25.01 Fnd: C 50.42 H 8.07 N 10.81 S 4.79 O
  • 24
  • [ 170215-68-6 ]
  • [ 114873-52-8 ]
  • [ 170215-87-9 ]
YieldReaction ConditionsOperation in experiment
6.93 g (51.6%) In ethanol; EXAMPLE 7a 1-[3-(N-Benzyl-mesylamino)-2-hydroxypropyl]-4,7,10-tris-(ethoxycarbonylmethyl)-1,4,7,10-tetraazacyclododecane 200 ml of absolute ethanol is poured over 8.61 g (20 mmol) of N,N',N"-tris-(ethoxycarbonylmethyl)-1,4,7,10-tetraazacyclododecane (produced according to DE 36 25 417 A1) in a bomb tube. After 4.83 g (20 mmol) of N-benzyl-N-[(2-oxiranyl)-methyl]-methanesulfonic acid amide is added (Example 2e), the bomb tube is closed, flushed with nitrogen, and the resulting reaction mixture is heated for 16 hours to 90 C. After the reaction (TLC control) is completed, the solvent is evaporated in a vacuum and the yellowish, oily residue is chromatographed on silica gel (eluent: chloroform/methanol; methanol: 0-80%). Yield: 6.93 g (51.6%), colorless oil Analysis: Relative to the anhydrous substance Cld: C 55.42 H 7.95 N 10.42 S 4.77 O 21.43 Fnd: C 55.31 H 7.72 N 10.37 S 4.48 O
  • 25
  • [ 170215-69-7 ]
  • [ 114873-52-8 ]
  • [ 170215-89-1 ]
YieldReaction ConditionsOperation in experiment
6.76 g (49.3%) In ethanol; EXAMPLE 8a 1-[3-(N-2-Phenylethyl-mesylamino)-2-hydroxypropyl]-4,7,10-tris-(ethoxycarbonylmethyl)-1,4,7,10-tetraazacyclododecane 200 ml of absolute ethanol is poured over 8.61 g (20 mmol) of N,N',N"-tris-(ethoxycarbonylmethyl)-1,4,7,10-tetraazacyclododecane (produced according to DE 36 25 417 A1) in a bomb tube. After 5.11 g (20 mmol) of N-(2-phenylethyl)-N-[(2-oxiranyl)-methyl]-methanesulfonic acid amide is added (Example 2f), the bomb tube is closed, flushed with nitrogen, and the resulting reaction mixture is heated for 16 hours to 90 C. After the reaction (TLC control) is completed, the solvent is evaporated in a vacuum and the yellowish, oily residue is chromatographed on silica gel (Eluent: chloroform/methanol; methanol: 0-80%). Yield: 6.76 g (49.3%), colorless oil Analysis: Relative to the anhydrous substance Cld: C 56.04 H 8.08 N 10.21 S 4.68 O 20.99 Fnd: C 55.86 H 7.93 N 10.14 S 4.57 O
  • 26
  • N-[(3,5-dioxa-4-phenyl-cyclohexyl)-methyl]-N-[(2-oxiranyl)-methyl]-methanesulfonic acid amide [ No CAS ]
  • [ 114873-52-8 ]
  • [ 170216-03-2 ]
YieldReaction ConditionsOperation in experiment
7.74 g (52.0%) In ethanol; EXAMPLE 15a 1-{3-[N-(3,5-Dioxa-4-phenyl-cyclohexyl)-mesylamino]-2-hydroxypropyl}-4,7,10-tris-(ethoxycarbonylmethyl)-1,4,7,10-tetraazacyclododecane 200 ml of absolute ethanol is poured over 8.61 g (20 mmol) of N,N',N"-tris-(ethoxycarbonylmethyl)-1,4,7,10-tetraazacyclododecane (produced according to DE 36 25 417 A1) in a bomb tube. After 6.27 g (20 mmol) of N-[(3,5-dioxa-4-phenyl-cyclohexyl)-methyl]-N-[(2-oxiranyl)-methyl]-methanesulfonic acid amide is added (Example 2m), the bomb tube is closed, flushed with nitrogen, and the resulting reaction mixture is heated for 16 hours to 90 C. After the reaction (TLC control) is completed, the solvent is evaporated in a vacuum and the yellowish, oily residue is chromatographed on silica gel (eluent: chloroform/methanol; methanol: 0-80%). Yield: 7.74 g (52.0%), colorless oil Analysis: Relative to the anhydrous substance Cld: C 54.89 H 7.72 N 9.41 S 4.31 O 23.66 Fnd: C 54.62 H 7.71 N 9.30 S 4.05 O
  • 27
  • [ 10361-91-8 ]
  • CH3OCOCH(CH2OH)NHCO2CH2C6H4OC5H5O(OCOCH3)3CH2OCOCH3 [ No CAS ]
  • [ 114873-52-8 ]
  • Yb(3+)*C8H16N4(CH2CO2)3CH(CO2)NHCO2CH2C6H4OC5H5O(OH)3CH2OH(4-)=YbC30H41N5O16(1-) [ No CAS ]
  • 28
  • [ 114873-52-8 ]
  • [ 54059-81-3 ]
  • triethyl 2,2',2"-(10-[2-(1-adamantylamino)-2-oxoethyl]-1,4,7,10-tetraazacyclododecane-1,4,7-triyl)triacetate [ No CAS ]
  • 29
  • [ 5292-43-3 ]
  • [ 114873-52-8 ]
  • 1,4,7-tris(ethoxycarbonylmethyl)-10-(tert-butoxycarbonylmethyl)-1,4,7,10-tetraazacyclododecane [ No CAS ]
  • 30
  • [6-(2-bromoacetylamino)hexyl]carbamic acid tert-butyl ester [ No CAS ]
  • [ 114873-52-8 ]
  • [ 1312681-65-4 ]
  • 31
  • 2-bromo-N-(3,7,12,16,20-pentamethylheneicosa-3,7,11,15,19-pentaenyl)acetamide [ No CAS ]
  • [ 114873-52-8 ]
  • triethyl 2,2',2''-[10-(2-oxo-2-[3,7,12,16,20-pentamethylheneicosa-3,7,11,15,19-pentaen-1-yl]amino}ethyl)-1,4,7,10-tetraazacyclododecane-1,4,7-triyl]triacetate [ No CAS ]
  • 32
  • 2-bromo-N-(4,8,12,17,21,25-hexamethyl-hexacosa-4,8,12,16,20,24-hexaenyl)acetamide [ No CAS ]
  • [ 114873-52-8 ]
  • {4,7-bis-ethoxycarbonylmethyl-10-[(4,8,12,17,21,25-hexamethylhexacosa-4,8,12,16,20,24-hexaenylcarbamoyl)methyl]-1,4,7,10-tetraazacyclododec-1-yl}acetic acid ethyl ester [ No CAS ]
  • 33
  • 2-bromo-N-(4,8,12,17,21,25-hexamethyl-hexacosa-4,8,12,16,20,24-hexaenyl)acetamide [ No CAS ]
  • [ 114873-52-8 ]
  • {4,7-bis-carboxymethyl-10-[(4,8,12,17,21,25-hexamethylhexacosa-4,8,12,16,20,24-hexaenylcarbamoyl)methyl]-1,4,7,10-tetraazacyclododec-1-yl}acetic acid [ No CAS ]
  • 34
  • [ 114873-52-8 ]
  • {4-[(6-aminohexylcarbamoyl)-methyl]-7,10-bis-ethoxycarbonylmethyl-1,4,7,10-tetraazacyclododec-1-yl}acetic acid ethyl ester [ No CAS ]
  • 35
  • [ 114873-52-8 ]
  • (4,7-bis-ethoxycarbonylmethyl-10-[6-(4,8,13,17,21-pentamethyldocosa-4,8,12,16,20-pentaenoylamino)hexylcarbamoyl]methyl}-1,4,7,10-tetraazacyclododec-1-yl)acetic acid ethyl ester [ No CAS ]
  • 36
  • [ 114873-52-8 ]
  • (4,7-bis-ethoxycarbonylmethyl-10-[6-(4,8,12,17,21,25-hexamethylhexacosa-4,8,12,16,20,24-hexaenoylamino)hexylcarbamoyl]methyl}-1,4,7,10-tetraazacyclododec-1-yl)acetic acid ethyl ester [ No CAS ]
  • 37
  • [ 114873-52-8 ]
  • (4,7-bis-carboxymethyl-10-[6-(4,8,13,17,21-pentamethyldocosa-4,8,12,16,20-pentaenoylamino)hexylcarbamoyl]methyl}-1,4,7,10-tetraazacyclododec-1-yl)acetic acid [ No CAS ]
  • 38
  • [ 114873-52-8 ]
  • (4,7-bis-carboxymethyl-10-[6-(4,8,12,17,21,25-hexamethylhexacosa-4,8,12,16,20,24-hexaenoylamino)hexylcarbamoyl]methyl}-1,4,7,10-tetraazacyclododec-1-yl)acetic acid [ No CAS ]
  • 39
  • [ 1361124-78-8 ]
  • [ 114873-52-8 ]
  • [ 1361124-79-9 ]
  • 40
  • [ 1361124-82-4 ]
  • [ 114873-52-8 ]
  • [ 1361124-81-3 ]
  • 41
  • [ 135924-27-5 ]
  • [ 114873-52-8 ]
  • [ 1361124-83-5 ]
  • 42
  • 2-bromo-1-(4-(((1,1,1,3,3,3-hexafluoropropan-2-yl)oxy)methoxy)phenyl)ethanone [ No CAS ]
  • [ 114873-52-8 ]
  • triethyl 2,2’,2’’-(10-(2-(4-(((1,1,1,3,3,3-hexafluoropropan-2-yl)oxy)methoxy)phenyl)-2-oxoethyl)-1,4,7,10-tetraazacyclododecane-1,4,7-triyl)triacetate [ No CAS ]
  • 43
  • 2-bromo-1-(4-(((1,1,1,3,3,3-hexafluoropropan-2-yl)oxy)methoxy)phenyl)ethanone [ No CAS ]
  • [ 114873-52-8 ]
  • 2,2’,2’’-(10-(2-(4-(((1,1,1,3,3,3-hexafluoropropan-2-yl)oxy)methoxy)phenyl)-2-oxoethyl)-1,4,7,10-tetraazacyclododecane-1,4,7-triyl)triacetic acid [ No CAS ]
  • 44
  • [ 114873-52-8 ]
  • 2,2',2''-(10-(2-oxo-2-(p-tolyl)ethyl)-1,4,7,10-tetraazacyclododecane-1,4,7-triyl)triacetic acid [ No CAS ]
  • 45
  • [ 619-41-0 ]
  • [ 114873-52-8 ]
  • triethyl 2,2',2''-(10-(2-oxo-2-(p-tolyl)ethyl)-1,4,7,10-tetraazacyclododecane-1,4,7-triyl)triacetate [ No CAS ]
  • 46
  • benzyl (6-(chloromethyl)pyridin-2-yl)carbamate [ No CAS ]
  • [ 114873-52-8 ]
  • triethyl 2,2',2''-(10-((6-(((benzyloxy)carbonyl)amino)pyridin-2-yl)methyl)-1,4,7,10-tetraazacyclododecane-1,4,7-triyl)triacetate [ No CAS ]
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