107336
2-硝基苄氯
99%
别名:
α-氯-2-硝基甲苯
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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:
210-300-5
Beilstein/REAXYS Number:
388396
MDL number:
产品名称
2-硝基苄氯, 99%
InChI key
BXCBUWKTXLWPSB-UHFFFAOYSA-N
InChI
1S/C7H6ClNO2/c8-5-6-3-1-2-4-7(6)9(10)11/h1-4H,5H2
SMILES string
[O-][N+](=O)c1ccccc1CCl
assay
99%
form
solid
bp
127-133 °C/10 mmHg (lit.)
mp
46-48 °C (lit.)
solubility
ethanol: soluble 98%
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Application
2-Nitrobenzyl chloride was used in the synthesis of S-(2-nitrobenzyl)cysteine which was inserted into human erythropoietin. 2-Nitrobenzyl chloride was used to prepare 4,4′-dinitrostillbene.
Biochem/physiol Actions
2-Nitrobenzyl chloride reacts with N-methyldiethanolamine and further reaction of the resulting quaternary diol with thionyl chloride at room temperature yields nitrobenzyl mustard quaternary salts.
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
233.6 °F
flash_point_c
112 °C
ppe
Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
法规信息
新产品
此项目有
Taek Jin Kang et al.
FEBS letters, 517(1-3), 211-214 (2002-06-14)
Using Escherichia coli cell-free protein synthesis system and aminoacylated amber suppressor tRNA, we successfully inserted an unnatural amino acid S-(2-nitrobenzyl)cysteine into human erythropoietin. Three different types of translation stop suppression were observed and each of the three types was easily
Influence of steric effects on the excited triplet-state lifetime of 2, 2'-dinitrostilbene and 2, 2', 4, 4', 6, 6'-hexanitrostilbene in acetonitrile solution.
Smit KJ.
The Journal of Physical Chemistry, 96(16), 6555-6558 (1992)
W A Denny et al.
International journal of radiation oncology, biology, physics, 29(2), 317-321 (1994-05-15)
To explore the utility of a new class of compounds, nitrobenzyl mustard quaternary salts, as hypoxia-selective prodrugs of diffusible cytotoxins. The parent compound N,N-bis(2-chloroethyl)-N-methyl-N-(2-nitrobenzyl)ammonium chloride (SN 25246) was prepared by reaction of 2-nitrobenzyl chloride with N-methyldiethanolamine, and reaction of the
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