191167
3-硝基苄氯
97%
别名:
α-氯-3-硝基甲苯
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关于此项目
线性分子式:
O2NC6H4CH2Cl
化学文摘社编号:
分子量:
171.58
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
210-586-1
Beilstein/REAXYS Number:
742794
MDL number:
产品名称
3-硝基苄氯, 97%
InChI key
APGGSERFJKEWFG-UHFFFAOYSA-N
InChI
1S/C7H6ClNO2/c8-5-6-2-1-3-7(4-6)9(10)11/h1-4H,5H2
SMILES string
[O-][N+](=O)c1cccc(CCl)c1
assay
97%
form
solid
bp
85-87 °C/5 mmHg (lit.)
mp
43-47 °C (lit.)
functional group
chloro
nitro
Quality Level
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Application
3-Nitrobenzyl chloride was used in the synthesis of 8-chloropurine.
General description
Influence of solvent on reduction mechanism of 3-nitrobenzyl chloride was investigated by cyclic voltammetry and controlled potential bulk electrolysis.
signalword
Danger
hcodes
Hazard Classifications
Eye Dam. 1 - Skin Corr. 1B
存储类别
8A - Combustible corrosive hazardous materials
wgk
WGK 3
flash_point_f
230.0 °F - closed cup
flash_point_c
110 °C - closed cup
ppe
Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
法规信息
新产品
此项目有
J L Kelley et al.
Journal of medicinal chemistry, 33(1), 196-202 (1990-01-01)
A series of 8-substituted analogues of 9-(3-aminobenzyl)-6-(dimethylamino)-9H-purine (8) were synthesized and tested for their ability to bind to the benzodiazepine receptor (BZR) in rat brain tissue. The most active compound was the 8-bromo-9-(3-formamidobenzyl) analogue 16 (IC50 = 0.011 microM), which
Solvent effects on the reduction mechanism of 3-chloroanthracene, 3-nitrobenzyl chloride and 3-chloroacetophenone.
Jensen H and Daasbjerg K
Acta Chirurgica Scandinavica. Supplementum, 58, 1151-1164 (1998)
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