365815
4-(Trifluoromethyl)benzyl chloride
98%
Synonym(s):
α′-Chloro-α,α,α-trifluoro-p-xylene
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5 G
$44.30
About This Item
Linear Formula:
CF3C6H4CH2Cl
CAS Number:
Molecular Weight:
194.58
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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Quality Level
assay
98%
form
liquid
refractive index
n20/D 1.464 (lit.)
bp
68 °C/12 mmHg (lit.)
density
1.315 g/mL at 25 °C (lit.)
functional group
chloro
fluoro
SMILES string
FC(F)(F)c1ccc(CCl)cc1
InChI
1S/C8H6ClF3/c9-5-6-1-3-7(4-2-6)8(10,11)12/h1-4H,5H2
InChI key
MCHDHQVROPEJJT-UHFFFAOYSA-N
Related Categories
General description
Electrochemical reduction of 4-(trifluoromethyl)benzyl chloride catalyzed by Co(salen) (H2salen, N,N′-bis(salicylidene)-ethane-1,2-diamine) in acetonitrile is reported.[1]
Application
4-(Trifluoromethyl)benzyl chloride may be used in the synthesis of novel series of dithiocarbamates, via reaction with sodium salts of N,N-disubstituted dithiocarbamic acids.[2]
signalword
Danger
hcodes
Hazard Classifications
Skin Corr. 1B - STOT SE 3
target_organs
Respiratory system
Storage Class
8A - Combustible corrosive hazardous materials
wgk_germany
WGK 3
flash_point_f
165.2 °F - closed cup
flash_point_c
74 °C - closed cup
ppe
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
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Mechanism of the electrochemical reduction of benzyl chlorides catalysed by Co (salen).
Isse AA, et al.
Journal of Electroanalytical Chemistry, 444(2), 241-245 (1992)
Mehlika D Altıntop et al.
Archiv der Pharmazie, 346(8), 571-576 (2013-07-25)
In the present paper, a novel series of dithiocarbamates was synthesized via the treatment of 4-(trifluoromethyl)benzyl chloride with appropriate sodium salts of N,N-disubstituted dithiocarbamic acids. The chemical structures of the compounds were elucidated by (1) H NMR, mass spectral data
Nicholas R Oranzi et al.
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