2-Chloro-3'4'-dimethoxybenzil

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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

Precursor & DownStream

Precursor

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

DownStream

  • 2''-Chloro-3,4-dimethoxybenzoin

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)


More Articles


Related Compounds

  • 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
  • N-{3-amino-4-[(tetrahydro-2H-pyran-4-ylmethyl)amino]phenyl}-N-methylbenzenesulfonamide
  • N-{3-Amino-4-[(2-cyclohexylethyl)amino]phenyl}-N-methylbenzenesulfonamide
  • N-{3-Amino-4-[(1-benzylpyrrolidin-3-yl)amino]phenyl}-N-methylbenzenesulfonamide
  • N-{3-Amino-4-[(cyclohexylmethyl)amino]phenyl}thiophene-2-sulfonamide
  • 4-Amino-N-[2-(1-methoxy-1-methylethyl)-1-(tetrahydro-2H-pyran-4-ylmethyl)-1H-benzimidazol-5-yl]-N-methylbenzenesulfonamide
  • Methyl (3-amino-4-{[(1-methylpiperidin-2-yl)methyl]amino}phenyl)carbamate
  • N-[4-[(cyclobutylmethyl)amino]-3-nitrophenyl]-benzenesulfonamide
  • N-{4-[(Cyclohexylmethyl)amino]-3-nitrophenyl}thiophene-2-sulfonamide
  • N-[4-({[2-tert-butyl-1-(2-hydroxyethyl)-1H-benzimidazol-5-yl]amino}sulfonyl)phenyl]acetamide
  • Methyl {3-amino-4-[(2-piperidin-1-ylethyl)amino]phenyl}carbamate
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