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Merck
CN

171778

Sigma-Aldrich

2-氨基苯并咪唑

97%

别名:

2-苯并咪唑胺

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About This Item

经验公式(希尔记法):
C7H7N3
CAS号:
分子量:
133.15
Beilstein:
116525
EC 号:
MDL编号:
UNSPSC代码:
12352100
eCl@ss:
32151902
PubChem化学物质编号:
NACRES:
NA.22

质量水平

检测方案

97%

形式

solid

mp

226-230 °C (lit.)

SMILES字符串

Nc1nc2ccccc2[nH]1

InChI

1S/C7H7N3/c8-7-9-5-3-1-2-4-6(5)10-7/h1-4H,(H3,8,9,10)

InChI key

JWYUFVNJZUSCSM-UHFFFAOYSA-N

基因信息

human ... PLAU(5328)

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应用

2-氨基苯并咪唑用于碳酸胆碱的水解 。它还用于咪唑并 [1,2-a] 苯并咪唑的合成

象形图

Exclamation mark

警示用语:

Warning

危险声明

危险分类

Acute Tox. 4 Oral

WGK

WGK 3

个人防护装备

dust mask type N95 (US), Eyeshields, Faceshields, Gloves


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Ya-Shan Hsiao et al.
ACS combinatorial science, 15(10), 551-555 (2013-09-11)
A one-pot, two-step synthesis of imidazo[1,2-a]benzimidazoles has been achieved by a three-component reaction of 2-aminobenzimidazoles with an aromatic aldehyde and an isocyanide. The reaction involving condensation of 2-aminobenzimidazole with an aldehyde is run under microwave activation to generate an imine
Bartolomé Soberats et al.
Organic letters, 16(3), 840-843 (2014-01-15)
The hydrolysis of a choline carbonate through a metal-free, enzyme-like mechanism has been achieved using a 2-aminobenzimidazole-based deep cavitand as catalyst. The supramolecular catalysis involves three steps: host-guest binding, carbamoylation and enzyme-like hydrolysis. Interestingly the rate-determining step proceeds through a
Timothy Coon et al.
Bioorganic & medicinal chemistry letters, 19(15), 4380-4384 (2009-06-26)
The benzimidazole core of the selective non-brain-penetrating H(1)-antihistamine mizolastine was used to identify a series of brain-penetrating H(1)-antihistamines for the potential treatment of insomnia. Using cassette PK studies, brain-penetrating H(1)-antihistamines were identified and in vivo efficacy was demonstrated in a
Kazuya Kikuchi et al.
Bioorganic & medicinal chemistry, 14(18), 6189-6196 (2006-06-20)
Antibodies that catalyze the deprotonation of unactivated benzisoxazoles to give the corresponding salicylonitriles were prepared using as antigen a 2-aminobenzimidazolium derivative coupled to a carrier protein via its benzene ring. The hapten was designed to induce an antibody binding site
2-Aminobenzimidazole derivatives strongly inhibit and disperse Pseudomonas aeruginosa biofilms.
Reto Frei et al.
Angewandte Chemie (International ed. in English), 51(21), 5226-5229 (2012-04-11)

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