2-Chloro-3'4'-dimethoxybenzil

Names

[ CAS No. ]:
56159-70-7

[ Name ]:
2-Chloro-3'4'-dimethoxybenzil

[Synonym ]:
2-Chlor-3',4'-dimethoxy-benzil
2-Chloro-3',4'-dimethoxybenzil
Benzil-based compound,23
MFCD00037469

Chemical & Physical Properties

[ Density]:
1.267 g/cm3

[ Boiling Point ]:
467.8ºC at 760 mmHg

[ Melting Point ]:
119-123ºC(lit.)

[ Molecular Formula ]:
C₁₆H₁₃ClO₄

[ Molecular Weight ]:
304.72500

[ Flash Point ]:
188ºC

[ Exact Mass ]:
304.05000

[ PSA ]:
52.60000

[ LogP ]:
3.42280

[ Index of Refraction ]:
1.575

MSDS

Safety Information

[ Symbol ]:

GHS07

[ Signal Word ]:
Warning

[ Hazard Statements ]:
H315-H319-H335

[ Precautionary Statements ]:
P261-P305 + P351 + P338

[ Personal Protective Equipment ]:
dust mask type N95 (US);Eyeshields;Gloves

[ Hazard Codes ]:
Xi: Irritant;

[ Risk Phrases ]:
R36/37/38

[ Safety Phrases ]:
26-36

[ RIDADR ]:
NONH for all modes of transport

Synthetic Route

Click to get detail synthetic route

Precursor & DownStream

Precursor

2''-Chloro-3,4-dimethoxybenzoin
benzene

DownStream

Articles

Stereoselective characteristics and mechanisms of epidermal carboxylesterase metabolism observed in HaCaT keratinocytes.

Biol. Pharm. Bull. 30(3) , 532-6, (2007)

There is increasing evidence that epidermal carboxylesterase may be involved in the stereoselective hydrolysis of prodrugs in percutaneous absorption. The present study was designed to evaluate the st...

2-(2-Chlorophenyl)-3-(3, 4-dimethoxyphenyl) quinoxaline. Cantalupo SA, et al.

Acta Crystallogr. Sect. E Struct. Rep. Online 66(8) , o2184-o2184., (2010)

Mixed benzoins. Ix. Meso chloro derivatives. Buck JS and Ide WS.

J. Am. Chem. Soc. 54(11) , 4359-4365, (1932)

2-chloro-10-[2-(diethylamino)ethyl]acridin-9-one
2-Chloro-4,5-difluoro-3-nitrobenzoic acid
2-chloro-5-phenylmethoxypyrazine
2-Chloro-5-methoxyquinoline
2-Chloro-4-ethylthiazole
2-Chloro-6-methoxynicotinaldehyde
3-[(3-chlorophenyl)sulfonyl]-N-(2-phenylethyl)thieno[2,3-e][1,2,3]triazolo[1,5-a]pyrimidin-5-amine
3-[(3-chlorophenyl)sulfonyl]-N-(2-methoxybenzyl)thieno[2,3-e][1,2,3]triazolo[1,5-a]pyrimidin-5-amine
3-[(3-Chlorophenyl)sulfonyl]-5-(1-pyrrolidinyl)thieno[2,3-e][1,2,3]triazolo[1,5-a]pyrimidine
2-[3-(anilinomethyl)-6,7-dimethoxy-2-oxoquinolin-1(2H)-yl]-N-(2,5-dimethylphenyl)acetamide
2-(6,7-dimethoxy-2-oxo-3-((phenylamino)methyl)quinolin-1(2H)-yl)-N-(m-tolyl)acetamide
2-{6,7-dimethoxy-2-oxo-3-[(phenylamino)methyl]-1,2-dihydroquinolin-1-yl}-N-(4-fluorophenyl)acetamide
2-{6,7-dimethoxy-2-oxo-3-[(phenylamino)methyl]-1,2-dihydroquinolin-1-yl}-N-(3-fluorophenyl)acetamide
N-(4-chlorophenyl)-2-{6,7-dimethoxy-2-oxo-3-[(phenylamino)methyl]-1,2-dihydroquinolin-1-yl}acetamide
N-(2-chlorophenyl)-2-{6,7-dimethoxy-2-oxo-3-[(phenylamino)methyl]-1,2-dihydroquinolin-1-yl}acetamide
2-(3-(((4-ethylphenyl)amino)methyl)-6,7-dimethoxy-2-oxoquinolin-1(2H)-yl)-N-(o-tolyl)acetamide

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