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(2-Chlorophenyl)phenyl-methanone

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(2-Chlorophenyl)phenyl-methanone Basic information

Product Name:
(2-Chlorophenyl)phenyl-methanone
Synonyms:
  • O-CHLOROBENZOPHENONE
  • RARECHEM AM UC 0602
  • LABOTEST-BB LT00159660
  • (2-chlorophenyl)phenyl-methanone
  • 2-CHLOROBENZOPHENONE
  • (2-chlorophenyl)phenyl-methanon
  • 2-Chlorobenzophenone/o-Chlorobenzophenone
  • 3-Chlorobenzophenone/m-Chlorobenzophenone
CAS:
5162-03-8
MF:
C13H9ClO
MW:
216.66
EINECS:
225-936-9
Product Categories:
  • Aromatics, Cross Linking Reagents, Metabolites & Impurities
  • Aromatic Benzophenones & Derivatives (substituted)
  • Functional Materials
  • Photopolymerization Initiators
  • C13 to C14
  • Carbonyl Compounds
  • Ketones
  • 5162-03-8
Mol File:
5162-03-8.mol
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(2-Chlorophenyl)phenyl-methanone Chemical Properties

Melting point:
44-47 °C(lit.)
Boiling point:
330 °C(lit.)
Density 
1,18g/cm
refractive index 
1.5260 (estimate)
Flash point:
>230 °F
storage temp. 
2-8°C
solubility 
Chloroform (Sparingly), Methanol (Slightly)
form 
Solid
color 
White to Off-White
BRN 
1869594
InChIKey
VMHYWKBKHMYRNF-UHFFFAOYSA-N
CAS DataBase Reference
5162-03-8(CAS DataBase Reference)
NIST Chemistry Reference
Methanone, (2-chlorophenyl)phenyl-(5162-03-8)
EPA Substance Registry System
Methanone, (2-chlorophenyl)phenyl- (5162-03-8)
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Safety Information

Hazard Codes 
Xi,Xn
Risk Statements 
36/37/38-20/21/22
Safety Statements 
37/39-26-24/25-36
WGK Germany 
3
RTECS 
PC4945633
Hazard Note 
Irritant
TSCA 
Yes
HS Code 
29143990

MSDS

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(2-Chlorophenyl)phenyl-methanone Usage And Synthesis

Chemical Properties

(2-Chlorophenyl)phenyl-methanone is white to yellow crystalline powder

Uses

(2-Chlorophenyl)phenyl-methanone is a metabolite of Clofedanol (C586920). Chlorobenzophenone is also used as a catalyst in the photocrosslinking of polyethylenes.

Uses

2-Chlorobenzophenone was used in the synthesis of 1-(2-chlorophenyl)isoquinolin-3-yl trifluoromethanesulfonate.

General Description

Thermodynamics of formation of inclusion complex between 2-chlorobenzophenone and cyclomaltoheptaose (β-cyclodextrin) has been investigated by UV-vis spectroscopy and reversed-phase liquid chromatography. 2-Chlorobenzophenone undergoes reduction in the presence of LiAlH4 and (R)-(-)-2-(2-iso-indolinyl)butan-1-ol to afford the corresponding benzhydrols.

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