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116416
1-Benzylimidazol
99%
Synonym(e):
1-(Phenylmethyl)-1H-imidazole, 1-Benzyl-1H-imidazole, N-Benzylimidazole
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5 G
CHF 35.20
25 G
CHF 74.40
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5 G
CHF 35.20
25 G
CHF 74.40
About This Item
Empirische Formel (Hill-System):
C10H10N2
CAS-Nummer:
Molekulargewicht:
158.20
Beilstein:
114571
EG-Nummer:
MDL-Nummer:
UNSPSC-Code:
12352005
eCl@ss:
39161001
PubChem Substanz-ID:
NACRES:
NA.22
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Assay
99%
bp
310 °C (lit.)
mp (Schmelzpunkt)
68-70 °C (lit.)
Funktionelle Gruppe
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
InChIKey
KKKDZZRICRFGSD-UHFFFAOYSA-N
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Verwandte Kategorien
Allgemeine Beschreibung
1-Benzylimidazole has been used to prepare cyclodextrin-ionic liquid polymer (βCD-BIMOTs-TDI)[1].
Biochem./physiol. Wirkung
1-Benzylimidazole is a CYP inhibitor that inhibits the biotransformation of MeO-BDEs (methoxylated-brominated diphenyl ethers) to OH-BDEs (hydroxylated) in fishes[2].
Lagerklassenschlüssel
11 - Combustible Solids
WGK
WGK 3
Flammpunkt (°F)
Not applicable
Flammpunkt (°C)
Not applicable
Persönliche Schutzausrüstung
Eyeshields, Gloves, type N95 (US)
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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
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
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
Guillaume Izzet et al.
Inorganic chemistry, 45(3), 1069-1077 (2006-01-31)
Complexation of copper(II) by calix[6]arene-based ligands bearing either two or three N-benzylimidazole coordinating arms under basic conditions has been studied. Whereas the tris(imidazole) derivative stabilizes dicationic 5-coordinate aqua complexes in a mononuclear state with an intracavity bound guest, in the
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