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Merck
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주요 문서

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116416

Sigma-Aldrich

1-Benzylimidazole

99%

동의어(들):

1-(Phenylmethyl)-1H-imidazole, 1-Benzyl-1H-imidazole, N-Benzylimidazole

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모든 사진(3)

About This Item

실험식(Hill 표기법):
C10H10N2
CAS Number:
4238-71-5
Molecular Weight:
158.20
Beilstein:
114571
EC Number:
224-200-4
MDL number:
MFCD00005296
UNSPSC 코드:
12352005
eCl@ss:
39161001
PubChem Substance ID:
24847290
NACRES:
NA.22

Quality Level

100

분석

99%

bp

310 °C (lit.)

mp

68-70 °C (lit.)

작용기

phenyl

SMILES string

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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관련 카테고리

일반 설명

1-Benzylimidazole has been used to prepare cyclodextrin-ionic liquid polymer (βCD-BIMOTs-TDI).

생화학적/생리학적 작용

1-Benzylimidazole is a CYP inhibitor that inhibits the biotransformation of MeO-BDEs (methoxylated-brominated diphenyl ethers) to OH-BDEs (hydroxylated) in fishes.

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point (°F)

Not applicable

Flash Point (°C)

Not applicable

개인 보호 장비

Eyeshields, Gloves, type N95 (US)

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시험 성적서(COA)

Lot/Batch Number
MKCK9688
MKBT2478V
MKBM7203V
MKBH8598V
MKBD5994

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문서 라이브러리 방문

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
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
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
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
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
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