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1-苯基咪唑

1-苯基咪唑用途

作药物原料，或有机合成。

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1-苯基咪唑名称

[ CAS 号 ]:
7164-98-9

[ 中文名 ]:
1-苯基咪唑

[ 英文名 ]:
1-Phenylimidazole

[中文别名 ]:

N-苯基咪唑

[英文别名 ]:

N-phenylimidazole
1H-Imidazole, 1-phenyl-
1-Phenyl imidazole
1H-Imidazole,1-phenyl
1-Phenyl-1H-imidazole
phenylimidazole
l-phenyl-1H-imidazole
MFCD00041204
1-phenylimidazole

1-苯基咪唑物理化学性质

[ 密度 ]:
1.1±0.1 g/cm3

[ 沸点 ]:
276.0±9.0 °C at 760 mmHg

[ 熔点 ]:
13 °C(lit.)

[ 分子式 ]:
C₉H₈N₂

[ 分子量 ]:
144.173

[ 闪点 ]:
120.7±18.7 °C

[ 精确质量 ]:
144.068741

[ PSA ]:
17.82000

[ LogP ]:
1.98

[ 外观性状 ]:
透明液体

[ 蒸汽压 ]:
0.0±0.5 mmHg at 25°C

[ 折射率 ]:
1.592

[ 储存条件 ]:
存放于惰性气体之中;避免空气

1-苯基咪唑MSDS

1-苯基咪唑安全信息

[ 符号 ]:

GHS07

[ 信号词 ]:
Warning

[ 危害声明 ]:
H302-H312-H315-H319-H332-H335

[ 警示性声明 ]:
P261-P280-P305 + P351 + P338

[ 个人防护装备 ]:
Eyeshields;Faceshields;full-face respirator (US);Gloves;multi-purpose combination respirator cartridge (US);type ABEK (EN14387) respirator filter

[ 危害码 (欧洲) ]:
Xn:Harmful;

[ 风险声明 (欧洲) ]:
R20/21/22;R36/37/38

[ 安全声明 (欧洲) ]:
S26-S37/39

[ 危险品运输编码 ]:
NONH for all modes of transport

[ WGK德国 ]:
3

[ 海关编码 ]:
2933290090

1-苯基咪唑合成路线

1-苯基咪唑上下游产品

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1-苯基咪唑海关

[ 海关编码 ]: 2933290090

[ 中文概述 ]:
2933290090. 其他结构含非稠合咪唑环的化合物. 增值税率:17.0%. 退税率:13.0%. 监管条件:无. 最惠国关税:6.5%. 普通关税:20.0%

[ 申报要素 ]: 品名, 成分含量, 用途, 乌洛托品请注明外观, 6－己内酰胺请注明外观, 签约日期

[ Summary ]:
2933290090. other compounds containing an unfused imidazole ring (whether or not hydrogenated) in the structure. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%

1-苯基咪唑文献

Influence of inhibition of the metabolic activation on the mutagenicity of some nitrosamines, triazenes, hydrazines and seniciphylline in Drosophila melanogaster.

Mutat. Res. 202(1) , 251-67, (1988)

It is determined to what extent certain inhibitors of the xenobiotic metabolizing enzyme systems have an influence on the mutagenicity of various pro-mutagens in Drosophila. 1-Phenylimidazole (PhI) is...

Calmodulin-dependent nitric-oxide synthase. Mechanism of inhibition by imidazole and phenylimidazoles.

J. Biol. Chem. 268(13) , 9425-9, (1993)

Calmodulin-dependent nitric-oxide synthase from bovine brain and GH3 pituitary cells is inhibited by imidazole, 1-phenylimidazole, 2-phenylimidazole, and 4-phenylimidazole, with half-maximal inhibitio...

Three-dimensional pharmacophore hypotheses for the locust neuronal octopamine receptor (OAR3). Part 2: agonists.

Bioorg. Med. Chem. 7(7) , 1437-43, (1999)

Three-dimensional pharmacophore hypotheses were built from a set of 43 agonists against octopamine receptor class 3 (OAR3) in locust nervous tissue. Among the 10 chemical-featured models generated by ...

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