Sign Into View Organizational & Contract Pricing
Select a Size
About This Item
Linear Formula:
(C6H5)2CHCl
CAS Number:
Molecular Weight:
202.68
Beilstein/REAXYS Number:
607925
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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.)
functional group
chloro
phenyl
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
Looking for similar products? Visit Product Comparison Guide
Related Categories
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.
signalword
Danger
hcodes
Hazard Classifications
Eye Dam. 1 - Skin Corr. 1B
Storage Class
8A - Combustible corrosive hazardous materials
wgk_germany
WGK 3
flash_point_f
233.6 °F - closed cup
flash_point_c
112 °C - closed cup
ppe
Eyeshields, Gloves, type ABEK (EN14387) respirator filter
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
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
Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
Contact Technical Service