All Photos(1)
Synonym(s):
Benzhydryl chloride, Diphenylchloromethane
Linear Formula:
(C6H5)2CHCl
CAS Number:
Molecular Weight:
202.68
Beilstein:
607925
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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Quality Level
Assay
98%
refractive index
n20/D 1.595 (lit.)
bp
140 °C/3 mmHg (lit.)
mp
15-17 °C (lit.)
density
1.14 g/mL at 25 °C (lit.)
SMILES string
ClC(c1ccccc1)c2ccccc2
InChI
1S/C13H11Cl/c14-13(11-7-3-1-4-8-11)12-9-5-2-6-10-12/h1-10,13H
InChI key
ZDVDCDLBOLSVGM-UHFFFAOYSA-N
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Application
Chlorodiphenylmethane was used as initiator during the controlled radical polymerization of styrene catalyzed by ionic iron complex. It was also used as the starting reagent in the synthesis of trimethylhydroquinone derivatives.
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Dam. 1 - Skin Corr. 1B
WGK
WGK 3
Flash Point(F)
233.6 °F
Flash Point(C)
112 °C
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
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Shota Niibayashi et al.
Chemical communications (Cambridge, England), (18)(18), 1855-1857 (2007-05-04)
Ionic iron complex [(Me(3)tacn)(2)Fe(2)Cl(3)](+)[(Me(3)tacn)FeCl(3)](-) (1), which is readily soluble in methanol, acted as a powerful catalyst in controlled radical polymerization of styrene and MMA, and showed promising features of removal from the resulting polymers and was reusable after recovery from
N Kawasaki et al.
Chemical & pharmaceutical bulletin, 47(2), 177-181 (1999-03-11)
A novel series of trimethylhydroquinone derivatives was synthesized and evaluated for their anti-lipid peroxidation activity in rat liver microsomes, inhibition of rat basophilic leukemia-1 (RBL-1) cell 5-lipoxygenase and 48 h homologous passive cutaneous anaphylaxis (PCA) activity in rats. 4-[4-[4-(Diphenylmethyl)-1-piperazinyl]-butoxy]-2,3,6-trimethyl phenol
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