[ CAS No. 62783-63-5 ] {[proInfo.proName]}

Name: 62783-63-5|Methyl 2-cyclohexyl-2-oxoacetate|97%
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SKU: A175461
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Quality Control of [ 62783-63-5 ]

COA NMR CNMR HPLC LC-MS

Related Doc. of [ 62783-63-5 ]

SDS Specification

Alternatived Products of [ 62783-63-5 ]

Product Details of [ 62783-63-5 ]

CAS No. :	62783-63-5	MDL No. :	MFCD24688272
Formula :	C₉H₁₄O₃	Boiling Point :	-
Linear Structure Formula :	-	InChI Key :	GLBPQIPSSQUXNZ-UHFFFAOYSA-N
M.W :	170.21	Pubchem ID :	11126698
Synonyms :

Calculated chemistry of [ 62783-63-5 ]

Physicochemical Properties

Num. heavy atoms :	12
Num. arom. heavy atoms :	0
Fraction Csp3 :	0.78
Num. rotatable bonds :	3
Num. H-bond acceptors :	3.0
Num. H-bond donors :	0.0
Molar Refractivity :	44.75
TPSA :	43.37 Å²

Pharmacokinetics

GI absorption :	High
BBB permeant :	Yes
P-gp substrate :	No
CYP1A2 inhibitor :	No
CYP2C19 inhibitor :	No
CYP2C9 inhibitor :	No
CYP2D6 inhibitor :	No
CYP3A4 inhibitor :	No
Log Kp (skin permeation) :	-5.86 cm/s

Lipophilicity

Log Po/w (iLOGP) :	2.05
Log Po/w (XLOGP3) :	2.08
Log Po/w (WLOGP) :	1.31
Log Po/w (MLOGP) :	0.9
Log Po/w (SILICOS-IT) :	1.67
Consensus Log Po/w :	1.6

Druglikeness

Lipinski :	0.0
Ghose :	None
Veber :	0.0
Egan :	0.0
Muegge :	1.0
Bioavailability Score :	0.55

Water Solubility

Log S (ESOL) :	-2.01
Solubility :	1.67 mg/ml ; 0.00982 mol/l
Class :	Soluble
Log S (Ali) :	-2.62
Solubility :	0.408 mg/ml ; 0.0024 mol/l
Class :	Soluble
Log S (SILICOS-IT) :	-1.34
Solubility :	7.85 mg/ml ; 0.0461 mol/l
Class :	Soluble

Medicinal Chemistry

PAINS :	0.0 alert
Brenk :	1.0 alert
Leadlikeness :	1.0
Synthetic accessibility :	1.77

Safety of [ 62783-63-5 ]

Signal Word:	Warning	Class:	N/A
Precautionary Statements:	P210-P273-P280-P305+P351+P338	UN#:	N/A
Hazard Statements:	H227-H302-H317-H319-H412	Packing Group:	N/A
GHS Pictogram:

Application In Synthesis of [ 62783-63-5 ]

* 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.

Upstream synthesis route of [ 62783-63-5 ]
Downstream synthetic route of [ 62783-63-5 ]

[ 62783-63-5 ] Synthesis Path-Upstream 1~5

1
[ 67-56-1 ]
[ 50284-86-1 ]
[ 62783-63-5 ]

Yield	Reaction Conditions	Operation in experiment
90%	With potassium permanganate; sodium hydrogencarbonate; magnesium sulfate In water at 0 - 20℃; for 2 h;	To a solution of 1 -chloro-2-cyclohexylethyne (0.50 mmol, purchased at ChemSampCo, Inc.) in MeOH (5ml) was added a solution of NaHC0₃ (23 mg, 0.28 mmol) and MgS0₄ (135mg, 1 .10 mmol) in water (5ml) at 0°C. The mixture was stirred for 10 min vigorously before KMn0₄ (260 mg, 1 .70 mmol) was added. The mixture was allowed to come to rt and stirred at this temperature for 2h. The solids were removed by filtration through celite pad and washed with ethyl acetate. The organic phase was separated and the aqueous phase was extracted with ethyl acetate ( 3X 100ml). The combined organic phases were washed with brine (30ml) and dried over MgS04. The solution was concentrated and then flash chromatographed using Hexane: EtOAc 5:1 to afford the corresponding a-ketoesters. Methyl 2-cyclohexyl-2-oxoacetate. (78 mg, 90percent) was obtained as a solid. TLC (Hexane: EtOAc 5:1 ): Rf = 0.40 MS (ESI) m/z 171 .49 [M + H] \ calculated 171 .16 [M + H] ⁺.

Reference： [1] Patent: WO2013/91900, 2013, A1, . Location in patent: Page/Page column 36

2
[ 99183-16-1 ]
[ 62783-63-5 ]

Reference： [1] Chemical Communications, 1999, # 15, p. 1387 - 1388
[2] Bioorganic and Medicinal Chemistry Letters, 2010, vol. 20, # 2, p. 632 - 635

3
[ 5781-53-3 ]
[ 931-50-0 ]
[ 62783-63-5 ]

Reference： [1] Tetrahedron, 1996, vol. 52, # 42, p. 13513 - 13520
[2] Patent: US2006/287322, 2006, A1, . Location in patent: Page/Page column 17

4
[ 553-90-2 ]
[ 108-85-0 ]
[ 62783-63-5 ]

Reference： [1] Chemical Communications, 2014, vol. 50, # 100, p. 15987 - 15990

5
[ 93343-82-9 ]
[ 74-88-4 ]
[ 4070-48-8 ]
[ 62783-63-5 ]
[ 93343-95-4 ]

Reference： [1] Tetrahedron, 1984, vol. 40, # 8, p. 1409 - 1418

[ 62783-63-5 ] Synthesis Path-Downstream 1~27

1
[ 62783-63-5 ]
[ 121099-13-6 ]
[ 92587-21-8 ]

Reference： [1]Tetrahedron Letters,1988,vol. 29,p. 5617 - 5620
[2]Journal of Organic Chemistry,1994,vol. 59,p. 3064 - 3076
[3]Journal of Organic Chemistry,1994,vol. 59,p. 3064 - 3076

2
[ 93343-82-9 ]
[ 74-88-4 ]
[ 4070-48-8 ]
[ 62783-63-5 ]
[ 93343-95-4 ]

Reference： [1]Tetrahedron,1984,vol. 40,p. 1409 - 1418

3
[ 5781-53-3 ]
[ 931-50-0 ]
[ 62783-63-5 ]

Yield	Reaction Conditions	Operation in experiment
65%		Example 14; Preparation of 7-(2-chlorophenyl)-8-(4-chlorophenyl)-3-cyclohexyl-4H-pyridazino[6,1-c][1,2,4]triazin-4-one; 14A. Preparation of methyl 2-cyclohexyl-2-oxoacetate; The title compound (1.1 g, 65%) as a colorless oil was prepared from cyclohexyl-magnesium bromide and methyl chlorooxoacetate by the procedures described in F. Babudri et al., Tetrahedron, 52 (42), pp. 13512-20 (1996).

Reference： [1]Tetrahedron,1996,vol. 52,p. 13513 - 13520
[2]Patent: US2006/287322,2006,A1 .Location in patent: Page/Page column 17

4
[ 99183-16-1 ]
[ 62783-63-5 ]

Reference： [1]Chemical Communications,1999,p. 1387 - 1388
[2]Bioorganic and Medicinal Chemistry Letters,2010,vol. 20,p. 632 - 635

6
[ 62783-63-5 ]
[ 557-20-0 ]
(R)-2-cyclohexyl-2-hydroxy-butyric acid methyl ester [ No CAS ]
(S)-2-cyclohexyl-2-hydroxy-butyric acid methyl ester [ No CAS ]

Reference： [1]Tetrahedron,2005,vol. 61,p. 6249 - 6265
[2]Chemical Communications,2017,vol. 53,p. 7513 - 7516

7
[ 62783-63-5 ]
[ 104-94-9 ]
cyclohexyl-(4-methoxy-phenylimino)-acetic acid methyl ester [ No CAS ]

Reference： [1]Angewandte Chemie - International Edition,2006,vol. 45,p. 6360 - 6362
[2]Advanced Synthesis and Catalysis,2010,vol. 352,p. 1846 - 1850

8
[ 62783-63-5 ]
[ 7393-43-3 ]
methyl (R)-2-cyclohexyl-2-hydroxypent-4-enoate [ No CAS ]
methyl 2-cyclohexyl-2-hydroxypent-4-enoate [ No CAS ]

Reference： [1]Journal of Organic Chemistry,2007,vol. 72,p. 8478 - 8483

9
[ 62783-63-5 ]
(+)-cyclohexyl-(4-methoxy-phenylamino)-acetic acid ethyl ester [ No CAS ]

Reference： [1]Angewandte Chemie - International Edition,2006,vol. 45,p. 6360 - 6362

10
[ 62783-63-5 ]
(-)-cyclohexyl-(4-methoxy-phenylamino)-acetic acid ethyl ester [ No CAS ]

Reference： [1]Angewandte Chemie - International Edition,2006,vol. 45,p. 6360 - 6362

11
[ 917486-09-0 ]
[ 62783-63-5 ]
7-(2-chlorophenyl)-8-(4-chlorophenyl)-3-cyclohexyl-4H-pyridazino[6,1-c][1,2,4]triazin-4-one [ No CAS ]

Yield	Reaction Conditions	Operation in experiment
74%	With acetic acid; at 120℃; for 1h;	14B. Preparation of 7-(2-chlorophenyl)-8-(4-chlorophenyl)-3-cyclohexyl-4H-pyridazino[6,1-c][1,2,4]triazin-4-one To a suspension of 1-(6-(2-chlorophenyl)-5-(4-chlorophenyl)pyridazin-3)hydrazine (50 mg, 0.15 mmol) in acetic acid (1 mL) was added <strong>[62783-63-5]methyl 2-cyclohexyl-2-oxoacetate</strong> (51 mg, 0.3 mmol). The reaction mixture was heated at 120 C. for 1 h. After cooling to room temperature, the reaction was concentrated under reduced pressure. The residue was diluted with EtOAc (30 mL), washed with water, saturated aqueous NaHCO3, saturated aqueous NaCl, dried (Na2SO4), filtered and concentrated under reduced pressure. The crude product was purified using a silica gel cartridge (12 g) eluding with a gradient of EtOAc (0-40%) in hexanes to afford 50 mg (74%) of the title compound as a pale yellow solid. LC/MS (method A): retention time=3.93 min, (M+H)+=451. 1H NMR (CDCl3, 400 MHz): delta 7.89 (s, 1H), 7.50-7.60 (m, 1H), 7.35-7.43 (m, 2H), 7.20-7.32 (m, 3H), 7.10 (d, 2H, J=12.0 Hz), 3.30-3.43 (m, 1H), 2.07 (d, 2H, J=12.0 Hz), 1.90 (d, 2H, J=12.0 Hz), 1.65-1.72 (m, 3H), 1.40-1.62 (m, 3H).

Reference： [1]Patent: US2006/287322,2006,A1 .Location in patent: Page/Page column 17-18

12
[ 62783-63-5 ]
[ 67-64-1 ]
C₁₂H₂₀O₄ [ No CAS ]
C₁₂H₂₀O₄ [ No CAS ]

Reference： [1]Advanced Synthesis and Catalysis,2007,vol. 349,p. 2665 - 2668

13
[ 62783-63-5 ]
[ 104-55-2 ]
C₁₈H₂₂O₄ [ No CAS ]
C₁₈H₂₂O₄ [ No CAS ]

Reference： [1]Advanced Synthesis and Catalysis,2008,vol. 350,p. 1885 - 1890

14
[ 7677-24-9 ]
[ 62783-63-5 ]
[ 1224978-79-3 ]
(S)-methyl 2-cyano-2-cyclohexyl-2-trimethylsiloxyacetate [ No CAS ]

Reference： [1]European Journal of Organic Chemistry,2010,p. 1455 - 1459

15
[ 62783-63-5 ]
[ 4354-49-8 ]

Reference： [1]Bioorganic and Medicinal Chemistry Letters,2010,vol. 20,p. 632 - 635
[2]Chemical Communications,2014,vol. 50,p. 15987 - 15990

16
[ 62783-63-5 ]
[ 6832-16-2 ]
(+)-dimethyl 2-cyclohexyl-3-diazo-2-hydroxysuccinate [ No CAS ]
(-)-dimethyl 2-cyclohexyl-3-diazo-2-hydroxysuccinate [ No CAS ]

Reference： [1]Chemical Communications,2009,p. 7297 - 7299

17
[ 67-56-1 ]
[ 50284-86-1 ]
[ 62783-63-5 ]

Yield	Reaction Conditions	Operation in experiment
90%	With potassium permanganate; sodium hydrogencarbonate; magnesium sulfate; In water; at 0 - 20℃; for 2h;	To a solution of 1 -chloro-2-cyclohexylethyne (0.50 mmol, purchased at ChemSampCo, Inc.) in MeOH (5ml) was added a solution of NaHC03 (23 mg, 0.28 mmol) and MgS04 (135mg, 1 .10 mmol) in water (5ml) at 0C. The mixture was stirred for 10 min vigorously before KMn04 (260 mg, 1 .70 mmol) was added. The mixture was allowed to come to rt and stirred at this temperature for 2h. The solids were removed by filtration through celite pad and washed with ethyl acetate. The organic phase was separated and the aqueous phase was extracted with ethyl acetate ( 3X 100ml). The combined organic phases were washed with brine (30ml) and dried over MgS04. The solution was concentrated and then flash chromatographed using Hexane: EtOAc 5:1 to afford the corresponding a-ketoesters. Methyl 2-cyclohexyl-2-oxoacetate. (78 mg, 90%) was obtained as a solid. TLC (Hexane: EtOAc 5:1 ): Rf = 0.40 MS (ESI) m/z 171 .49 [M + H] calculated 171 .16 [M + H] +.

Reference： [1]Patent: WO2013/91900,2013,A1 .Location in patent: Page/Page column 36

18
[ 62783-63-5 ]
[ 146896-52-8 ]
[ 1616777-70-8 ]

Reference： [1]Chemical Communications,2014,vol. 50,p. 7524 - 7526

19
[ 553-90-2 ]
[ 108-85-0 ]
[ 62783-63-5 ]

Reference： [1]Chemical Communications,2014,vol. 50,p. 15987 - 15990

20
[ 62783-63-5 ]
[ 16640-68-9 ]
(Z)-methyl 3-cyano-2-cyclohexylacrylate [ No CAS ]
(E)-methyl 3-cyano-2-cyclohexylacrylate [ No CAS ]

Reference： [1]Organic and Biomolecular Chemistry,2016,vol. 14,p. 1216 - 1220

21
[ 62783-63-5 ]
methyl 3-cyano-2-cyclohexylpropanoate [ No CAS ]

Reference： [1]Organic and Biomolecular Chemistry,2016,vol. 14,p. 1216 - 1220

22
[ 62783-63-5 ]
methyl 3-cyano-2-cyclohexylpropanoate [ No CAS ]

Reference： [1]Organic and Biomolecular Chemistry,2016,vol. 14,p. 1216 - 1220

23
[ 62783-63-5 ]
[ 99183-16-1 ]

Yield	Reaction Conditions	Operation in experiment
94%	With carbonylhydrido(tetrahydroborato)[bis(2-diphenylphosphinoethyl)-amino]ruthenium(II); hydrogen; sodium hydrogencarbonate; In methanol; at 25℃; under 7500.75 Torr; for 12h;Glovebox; Autoclave;	General procedure: A glass liner containing a stir bar was charged with substrate (0.5 mmol), base (0.05mmol), Ru-MACHO (5 umol) and MeOH (0.5 mL) in a glove box. The glass linerwas then placed into an autoclave followed by degassing with H2 three times. Thehydrogenation was carried out at 10-50 bar H2 with stirring at 25oC or 80oC for 12-24h. After the reaction finished, the autoclave was allowed to cool down to r.t. Thehydrogen gas was then carefully released in a fume hood, and the solution transferredto a flask with H2O (2 ml), extracted with EA (3x5 ml), dried with Na2SO4 andconcentrated in vacuo to afford the pure product 2a-2s or 3a-3s.

Reference： [1]Synlett,2016,vol. 27,p. 1748 - 1752
[2]ChemCatChem,2016,vol. 8,p. 571 - 576

24
[ 62783-63-5 ]
[ 61414-09-3 ]

Yield	Reaction Conditions	Operation in experiment
91%	With carbonylhydrido(tetrahydroborato)[bis(2-diphenylphosphinoethyl)-amino]ruthenium(II); hydrogen; sodium t-butanolate; In methanol; at 80℃; under 37503.8 Torr; for 12h;Glovebox; Autoclave;	General procedure: A glass liner containing a stir bar was charged with substrate (0.5 mmol), base (0.05mmol), Ru-MACHO (5 umol) and MeOH (0.5 mL) in a glove box. The glass linerwas then placed into an autoclave followed by degassing with H2 three times. Thehydrogenation was carried out at 10-50 bar H2 with stirring at 25oC or 80oC for 12-24h. After the reaction finished, the autoclave was allowed to cool down to r.t. Thehydrogen gas was then carefully released in a fume hood, and the solution transferredto a flask with H2O (2 ml), extracted with EA (3x5 ml), dried with Na2SO4 andconcentrated in vacuo to afford the pure product 2a-2s or 3a-3s.

Reference： [1]Synlett,2016,vol. 27,p. 1748 - 1752

25
[ 62783-63-5 ]
[ 72824-04-5 ]
methyl (R)-2-cyclohexyl-2-hydroxypent-4-enoate [ No CAS ]

Reference： [1]Angewandte Chemie - International Edition,2016,vol. 55,p. 9610 - 9614
Angew. Chem.,2016,vol. 128,p. 9762 - 9766,5

26
[ 62783-63-5 ]
[ 70-11-1 ]
[ 55846-70-3 ]

Reference： [1]Journal of Organic Chemistry,2017,vol. 82,p. 1403 - 1411

27
[ 62783-63-5 ]
C₁₀H₁₈O₂Si [ No CAS ]
(2E,4E)-dimethyl 7-cyclohexyl-7-hydroxyocta-2,4-dienedioate [ No CAS ]
C₁₆H₂₄O₅ [ No CAS ]

Reference： [1]Organic Letters,2017,vol. 19,p. 332 - 335

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Ghs Precautionary Statements

Precautionary Statements-General
Code	Phrase
P101	If medical advice is needed,have product container or label at hand.
P102	Keep out of reach of children.
P103	Read label before use
Prevention
Code	Phrase
P201	Obtain special instructions before use.
P202	Do not handle until all safety precautions have been read and understood.
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P220	Keep/Store away from clothing/combustible materials.
P221	Take any precaution to avoid mixing with combustibles
P222	Do not allow contact with air.
P223	Keep away from any possible contact with water, because of violent reaction and possible flash fire.
P230	Keep wetted
P231	Handle under inert gas.
P232	Protect from moisture.
P233	Keep container tightly closed.
P234	Keep only in original container.
P235	Keep cool
P240	Ground/bond container and receiving equipment.
P241	Use explosion-proof electrical/ventilating/lighting/equipment.
P242	Use only non-sparking tools.
P243	Take precautionary measures against static discharge.
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P251	Pressurized container: Do not pierce or burn, even after use.
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P270	Do not eat, drink or smoke when using this product.
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P281	Use personal protective equipment as required.
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P284	Wear respiratory protection.
P285	In case of inadequate ventilation wear respiratory protection.
P231 + P232	Handle under inert gas. Protect from moisture.
P235 + P410	Keep cool. Protect from sunlight.
Response
Code	Phrase
P301	IF SWALLOWED:
P304	IF INHALED:
P305	IF IN EYES:
P306	IF ON CLOTHING:
P307	IF exposed:
P308	IF exposed or concerned:
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P310	Immediately call a POISON CENTER or doctor/physician.
P311	Call a POISON CENTER or doctor/physician.
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P313	Get medical advice/attention.
P314	Get medical advice/attention if you feel unwell.
P315	Get immediate medical advice/attention.
P320
P302 + P352	IF ON SKIN: wash with plenty of soap and water.
P321
P322
P330	Rinse mouth.
P331	Do NOT induce vomiting.
P332	IF SKIN irritation occurs:
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P341	If breathing is difficult, remove victim to fresh air and keep at rest in a position comfortable for breathing.
P342	If experiencing respiratory symptoms:
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P351	Rinse cautiously with water for several minutes.
P352	Wash with plenty of soap and water.
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P374	Fight fire with normal precautions from a reasonable distance.
P376	Stop leak if safe to do so. Oxidising gases (section 2.4) 1
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P378
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P390	Absorb spillage to prevent material damage.
P391	Collect spillage. Hazardous to the aquatic environment
P301 + P310	IF SWALLOWED: Immediately call a POISON CENTER or doctor/physician.
P301 + P312	IF SWALLOWED: call a POISON CENTER or doctor/physician IF you feel unwell.
P301 + P330 + P331	IF SWALLOWED: Rinse mouth. Do NOT induce vomiting.
P302 + P334	IF ON SKIN: Immerse in cool water/wrap in wet bandages.
P302 + P350	IF ON SKIN: Gently wash with plenty of soap and water.
P303 + P361 + P353	IF ON SKIN (or hair): Remove/Take off Immediately all contaminated clothing. Rinse SKIN with water/shower.
P304 + P312	IF INHALED: Call a POISON CENTER or doctor/physician if you feel unwell.
P304 + P340	IF INHALED: Remove victim to fresh air and Keep at rest in a position comfortable for breathing.
P304 + P341	IF INHALED: If breathing is difficult, remove victim to fresh air and keep at rest in a position comfortable for breathing.
P305 + P351 + P338	IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continue rinsing.
P306 + P360	IF ON CLOTHING: Rinse Immediately contaminated CLOTHING and SKIN with plenty of water before removing clothes.
P307 + P311	IF exposed: call a POISON CENTER or doctor/physician.
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P309 + P311	IF exposed or if you feel unwell: call a POISON CENTER or doctor/physician.
P332 + P313	IF SKIN irritation occurs: Get medical advice/attention.
P333 + P313	IF SKIN irritation or rash occurs: Get medical advice/attention.
P335 + P334	Brush off loose particles from skin. Immerse in cool water/wrap in wet bandages.
P337 + P313	IF eye irritation persists: Get medical advice/attention.
P342 + P311	IF experiencing respiratory symptoms: call a POISON CENTER or doctor/physician.
P370 + P376	In case of fire: Stop leak if safe to Do so.
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P401
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P422
P402 + P404	Store in a dry place. Store in a closed container.
P403 + P233	Store in a well-ventilated place. Keep container tightly closed.
P403 + P235	Store in a well-ventilated place. Keep cool.
P410 + P403	Protect from sunlight. Store in a well-ventilated place.
P410 + P412	Protect from sunlight. Do not expose to temperatures exceeding 50 oC/122oF.
P411 + P235	Keep cool.
Disposal
Code	Phrase
P501	Dispose of contents/container to ...
P502	Refer to manufacturer/supplier for information on recovery/recycling

Purity	Size	Price	VIP Price	USA Stock *0-1 Day	Global Stock *5-7 Days	Quantity
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Physical hazards
Code	Phrase
H200	Unstable explosive
H201	Explosive; mass explosion hazard
H202	Explosive; severe projection hazard
H203	Explosive; fire, blast or projection hazard
H204	Fire or projection hazard
H205	May mass explode in fire
H220	Extremely flammable gas
H221	Flammable gas
H222	Extremely flammable aerosol
H223	Flammable aerosol
H224	Extremely flammable liquid and vapour
H225	Highly flammable liquid and vapour
H226	Flammable liquid and vapour
H227	Combustible liquid
H228	Flammable solid
H229	Pressurized container: may burst if heated
H230	May react explosively even in the absence of air
H231	May react explosively even in the absence of air at elevated pressure and/or temperature
H240	Heating may cause an explosion
H241	Heating may cause a fire or explosion
H242	Heating may cause a fire
H250	Catches fire spontaneously if exposed to air
H251	Self-heating; may catch fire
H252	Self-heating in large quantities; may catch fire
H260	In contact with water releases flammable gases which may ignite spontaneously
H261	In contact with water releases flammable gas
H270	May cause or intensify fire; oxidizer
H271	May cause fire or explosion; strong oxidizer
H272	May intensify fire; oxidizer
H280	Contains gas under pressure; may explode if heated
H281	Contains refrigerated gas; may cause cryogenic burns or injury
H290	May be corrosive to metals
Health hazards
Code	Phrase
H300	Fatal if swallowed
H301	Toxic if swallowed
H302	Harmful if swallowed
H303	May be harmful if swallowed
H304	May be fatal if swallowed and enters airways
H305	May be harmful if swallowed and enters airways
H310	Fatal in contact with skin
H311	Toxic in contact with skin
H312	Harmful in contact with skin
H313	May be harmful in contact with skin
H314	Causes severe skin burns and eye damage
H315	Causes skin irritation
H316	Causes mild skin irritation
H317	May cause an allergic skin reaction
H318	Causes serious eye damage
H319	Causes serious eye irritation
H320	Causes eye irritation
H330	Fatal if inhaled
H331	Toxic if inhaled
H332	Harmful if inhaled
H333	May be harmful if inhaled
H334	May cause allergy or asthma symptoms or breathing difficulties if inhaled
H335	May cause respiratory irritation
H336	May cause drowsiness or dizziness
H340	May cause genetic defects
H341	Suspected of causing genetic defects
H350	May cause cancer
H351	Suspected of causing cancer
H360	May damage fertility or the unborn child
H361	Suspected of damaging fertility or the unborn child
H361d	Suspected of damaging the unborn child
H362	May cause harm to breast-fed children
H370	Causes damage to organs
H371	May cause damage to organs
H372	Causes damage to organs through prolonged or repeated exposure
H373	May cause damage to organs through prolonged or repeated exposure
Environmental hazards
Code	Phrase
H400	Very toxic to aquatic life
H401	Toxic to aquatic life
H402	Harmful to aquatic life
H410	Very toxic to aquatic life with long-lasting effects
H411	Toxic to aquatic life with long-lasting effects
H412	Harmful to aquatic life with long-lasting effects
H413	May cause long-lasting harmful effects to aquatic life
H420	Harms public health and the environment by destroying ozone in the upper atmosphere

[ CAS No. 62783-63-5 ] {[proInfo.proName]}

Quality Control of [ 62783-63-5 ]

Related Doc. of [ 62783-63-5 ]

Product Details of [ 62783-63-5 ]

Calculated chemistry of [ 62783-63-5 ]

Physicochemical Properties

Pharmacokinetics

Lipophilicity

Druglikeness

Water Solubility

Medicinal Chemistry

Safety of [ 62783-63-5 ]

Application In Synthesis of [ 62783-63-5 ]

[ 62783-63-5 ] Synthesis Path-Upstream 1~5

[ 62783-63-5 ] Synthesis Path-Downstream 1~27

Related Functional Groups of [ 62783-63-5 ]

Aliphatic Cyclic Hydrocarbons

Esters

Ketones

Precautionary Statements-General

Prevention

Response

Storage

Disposal

Physical hazards

Health hazards

Environmental hazards

Inquiry

Related Functional Groups of
[ 62783-63-5 ]