115886
间氯氯苄
98%
别名:
α,3-二氯甲苯
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线性分子式:
ClC6H4CH2Cl
化学文摘社编号:
分子量:
161.03
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
210-629-4
Beilstein/REAXYS Number:
742266
MDL number:
产品名称
间氯氯苄, 98%
InChI key
DDGRAFHHXYIQQR-UHFFFAOYSA-N
InChI
1S/C7H6Cl2/c8-5-6-2-1-3-7(9)4-6/h1-4H,5H2
SMILES string
ClCc1cccc(Cl)c1
assay
98%
refractive index
n20/D 1.555 (lit.)
bp
215-216 °C (lit.)
density
1.27 g/mL at 25 °C (lit.)
functional group
chloro
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Application
3-Chlorobenzyl chloride has been used in the reaction of 3-methoxybenzyl chloride and ethyl 4-bromobenzoate in pure water, using zinc dust and a Pd catalyst.
signalword
Danger
hcodes
Hazard Classifications
Skin Corr. 1B
存储类别
6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
wgk
WGK 3
flash_point_f
208.4 °F - closed cup
flash_point_c
98 °C - closed cup
ppe
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
Christophe Duplais et al.
Chemical communications (Cambridge, England), 46(4), 562-564 (2010-01-12)
A remarkably simple entry to unsymmetrical diarylmethanes has been developed that relies on an in situ organozinc-mediated, palladium-catalyzed cross-coupling. Thus, by mixing a benzyl and aryl halide together in the presence of Zn metal and a Pd catalyst, diarylmethanes are
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