145467
邻氯苄醇
99%
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线性分子式:
ClC6H4CH2OH
化学文摘社编号:
分子量:
142.58
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
241-801-7
Beilstein/REAXYS Number:
2042182
MDL number:
产品名称
邻氯苄醇, 99%
InChI key
MBYQPPXEXWRMQC-UHFFFAOYSA-N
InChI
1S/C7H7ClO/c8-7-4-2-1-3-6(7)5-9/h1-4,9H,5H2
SMILES string
OCc1ccccc1Cl
assay
99%
form
solid
bp
227 °C (lit.)
mp
69-71 °C (lit.)
solubility
chloroform: soluble 25 mg/mL, clear, colorless
functional group
chloro
hydroxyl
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General description
大鼠2-氯苄醇的主要尿代谢产物为2-氯马尿酸、2-氯苄基半胱氨酸、2-氯苯甲酸和2-氯苄基葡萄糖醛酸。它是2-氯扁桃酸代谢过程中可能形成的一种中间体。
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
K Brewster et al.
Xenobiotica; the fate of foreign compounds in biological systems, 17(8), 911-924 (1987-08-01)
1. The fate of 3H-ring labelled, 14C-cyanide labelled and (14C = C) side chain labelled 2-chlorobenzylidene malononitrile (CS), 2-chlorobenzyl alcohol and 2-chlorobenzyl malononitrile (dihydro CS) in rats and isolated rat liver cells has been examined. 2. CS was administered both
G S J Mannens et al.
Drug metabolism and disposition: the biological fate of chemicals, 35(4), 554-565 (2006-08-29)
RWJ-333369 (1,2-ethanediol, [1-2-chlorophenyl]-, 2-carbamate, [S]-; CAS Registry Number 194085-75-1) is a novel neuromodulator in clinical development for the treatment of epilepsy. To study the disposition of RWJ-333369, eight healthy male subjects received a single oral dose of 500 mg of
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