116416
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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关于此项目
经验公式（希尔记法）:
C10H10N2
化学文摘社编号:
分子量:
158.20
Beilstein:
114571
EC 号:
MDL编号:
UNSPSC代码:
12352005
eCl@ss:
39161001
PubChem化学物质编号:
NACRES:
NA.22
质量水平
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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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)
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
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
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
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
Muggundha Raoov et al.
Journal of hazardous materials, 263 Pt 2, 501-516 (2013-11-16)
Cyclodextrin-ionic liquid polymer (βCD-BIMOTs-TDI) was firstly synthesized using functionalized β-Cyclodextrin (CD) with 1-benzylimidazole (BIM) to form monofunctionalized CD (βCD-BIMOTs) and was further polymerized using toluene diisocyanate (TDI) linker to form insoluble βCD-BIMOTs-TDI. SEM characterization result shows that βCD-BIMOTs-TDI exhibits macropore
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