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116416

Sigma-Aldrich

1-苄基咪唑

99%

别名:

1-苄基-1H-咪唑, 1-（苯甲基）-1H-咪唑, N-苄基咪唑

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About This Item

经验公式（希尔记法）:
C10H10N2
CAS号:
4238-71-5
分子量:
158.20
Beilstein:
114571
EC 号:
224-200-4
MDL编号:
MFCD00005296
UNSPSC代码:
12352005
eCl@ss:
39161001
PubChem化学物质编号:
24847290
NACRES:
NA.22

质量水平

100

方案

99%

沸点

310 °C (lit.)

mp

68-70 °C (lit.)

官能团

phenyl

SMILES字符串

C(c1ccccc1)n2ccnc2

InChI

1S/C10H10N2/c1-2-4-10(5-3-1)8-12-7-6-11-9-12/h1-7,9H,8H2

InChI key

KKKDZZRICRFGSD-UHFFFAOYSA-N

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相关类别

一般描述

1-苄基咪唑已被用于制备环糊精-离子液体聚合物（βCD-BIMOTs-TDI）。

生化/生理作用

1-苄咪唑是一种 CYP 抑制剂，可抑制鱼类中 MeO-BDEs（甲氧基-溴代二苯醚）生物转化为 OH-BDEs（羟基化）。

储存分类代码

11 - Combustible Solids

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

Eyeshields, Gloves, type N95 (US)

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number
MKCK9688
MKBT2478V
MKBM7203V
MKBH8598V
MKBD5994

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P Rothenbach et al.
Journal of applied physiology (Bethesda, Md. : 1985), 83(2), 530-536 (1997-08-01)
This study examines the hypothesis that intestinal ischemia-reperfusion (I/R) injury contributes to renal dysfunction by altered renal eicosanoid release. Anesthetized Sprague-Dawley rats underwent 60 min of sham or superior mesenteric artery (SMA) occlusion with 60 min of reperfusion. The I/R
K V Dileep et al.
International journal of biological macromolecules, 170, 415-423 (2020-12-30)
Alzheimer's disease (AD), a common chronic neurodegenerative disease, has become a major public health concern. Despite years of research, therapeutics for AD are limited. Overexpression of secretory glutaminyl cyclase (sQC) in AD brain leads to the formation of a highly
A Grothusen et al.
Archives of toxicology, 71(1-2), 64-71 (1996-01-01)
Liver microsomes are a frequently used probe to investigate the phase I metabolism of xenobiotics in vitro. Structures containing nucleophilic hetero-atoms are possible substrates for cytochrome P450 enzymes (P450) and flavin-containing monooxygenases (FMO). Both enzymes are located in the endoplasmatic
Jérémie Doiron et al.
European journal of medicinal chemistry, 46(9), 4010-4024 (2011-06-28)
A series of bis- and mono-benzonitrile or phenyl analogues of letrozole 1, bearing (1,2,3 and 1,2,5)-triazole or imidazole, were synthesized and screened for their anti-aromatase activities. The unsubstituted 1,2,3-triazole 10a derivative displayed inhibitory activity comparable with that of the aromatase
José María Navas et al.
Environmental toxicology and chemistry, 22(4), 830-836 (2003-04-11)
Xenobiotics can induce cytochrome P4501A (CYP1A) by ligand binding to the aryl hydrocarbon receptor (AhR). Typical AhR ligands are polycyclic aromatic compounds with planar molecular conformation. The present work investigated the ability of the N-imidazole derivative, 1-benzylimidazole (BIM), to induce
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