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4-苯基咪唑

4-苯基咪唑用途

4-苯基咪唑是一种生物化学试剂,可作为生物材料或有机化合物用于生命科学相关研究。

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4-苯基咪唑名称

[ CAS 号 ]:
670-95-1

[ 中文名 ]:
4-苯基咪唑

[ 英文名 ]:
4-PHENYLIMIDAZOLE

[中文别名 ]:

4-苯咪唑

[英文别名 ]:

EINECS 211-580-1
MFCD00005197
5-phenyl-1H-imidazole
1H-Imidazole, 4-phenyl-
4-Phenylimidazole
4-Phenyl-1H-imidazole

4-苯基咪唑生物活性

[ 描述 ]:

4-苯基咪唑是一种生物化学试剂,可作为生物材料或有机化合物用于生命科学相关研究。

[ 相关类别 ]:

研究领域 >> 其他

信号通路 >> 其他 >> 其他

4-苯基咪唑物理化学性质

[ 密度 ]:
1.1±0.1 g/cm3

[ 沸点 ]:
379.8±11.0 °C at 760 mmHg

[ 熔点 ]:
128-131 °C(lit.)

[ 分子式 ]:
C₉H₈N₂

[ 分子量 ]:
144.17

[ 闪点 ]:
213.0±5.7 °C

[ 精确质量 ]:
144.068741

[ PSA ]:
28.68000

[ LogP ]:
1.46

[ 外观性状 ]:
白色粉末

[ 蒸汽压 ]:
0.0±0.8 mmHg at 25°C

[ 折射率 ]:
1.603

[ 储存条件 ]:
室温，密封，干燥

4-苯基咪唑MSDS

4-苯基咪唑安全信息

[ 符号 ]:

GHS07

[ 信号词 ]:
Warning

[ 危害声明 ]:
H315-H319-H335

[ 警示性声明 ]:
P261-P305 + P351 + P338

[ 个人防护装备 ]:
dust mask type N95 (US);Eyeshields;Gloves

[ 危害码 (欧洲) ]:
Xi

[ 风险声明 (欧洲) ]:
R36/37/38

[ 安全声明 (欧洲) ]:
S26-S36-S24/25

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

[ WGK德国 ]:
3

[ 海关编码 ]:
2933290090

4-苯基咪唑合成路线

4-苯基咪唑上下游产品

4-苯基咪唑上游产品

4-苯基咪唑下游产品

4-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%

4-苯基咪唑文献

Novel synthetic pyridyl analogues of CDDO-Imidazolide are useful new tools in cancer prevention.

Pharmacol. Res. 100 , 135-47, (2015)

Two new analogues of CDDO-Imidazolide (CDDO-Im), namely 1-[2-Cyano-3,12-dioxooleana-1,9(11)-dien-28-oyl]-4(-pyridin-2-yl)-1H-imidazole ("CDDO-2P-Im") and 1-[2-Cyano-3,12-dioxooleana-1,9(11)-dien-28-oy...

Small-molecule scaffolds for CYP51 inhibitors identified by high-throughput screening and defined by X-ray crystallography.

Antimicrob. Agents Chemother. 51 , 3915-23, (2007)

Sterol 14alpha-demethylase (CYP51), a major checkpoint in membrane sterol biosynthesis, is a key target for fungal antibiotic therapy. We sought small organic molecules for lead candidate CYP51 inhibi...

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...

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