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116416

Sigma-Aldrich

1-苄基咪唑

99%

同義詞:

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

經驗公式（希爾表示法）:
C10H10N2
CAS號碼:
4238-71-5
分子量：:
158.20
Beilstein:
114571
EC號碼:
224-200-4
MDL號碼:
MFCD00005296
分類程式碼代碼:
12352005
eCl@ss:
39161001
PubChem物質ID:
24847290
NACRES:
NA.22

品質等級

100

化驗

99%

bp

310 °C (lit.)

mp

68-70 °C (lit.)

官能基

phenyl

SMILES 字串

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 密鑰

KKKDZZRICRFGSD-UHFFFAOYSA-N

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相關類別

一般說明

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）。

儲存類別代碼

11 - Combustible Solids

水污染物質分類（WGK）

WGK 3

閃點（°F）

Not applicable

閃點（°C）

Not applicable

個人防護裝備

Eyeshields, Gloves, type N95 (US)

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分析證明 (COA)

Lot/Batch Number
MKCK9688
MKBT2478V
MKBM7203V
MKBH8598V
MKBD5994

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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
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
Fredrik Jernerén et al.
Lipids, 47(7), 707-717 (2012-05-01)
(8R)-Hydroperoxy-(9Z,12Z)-octadecadienoic acid (8-HPODE) is formed by aspergilli as an intermediate in biosynthesis of oxylipins with effects on sporulation. 8-HPODE is transformed by separate diol synthases to (5S,8R)-dihydroxy- and (8R,11S)-dihydroxy-(9Z,12Z)-octadecadienoic acids (5,8- and 8,11-DiHODE). The former is formed by the cytochrome
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