主要文件

查看所有文档

171778

2-氨基苯并咪唑

Name: 2-氨基苯并咪唑
Brand: ALDRICH

97%

别名:

2-苯并咪唑胺

登录查看组织和合同定价。

选择尺寸

变更视图

关于此项目

经验公式（希尔记法）:

C₇H₇N₃

化学文摘社编号:

934-32-7

分子量:

133.15

NACRES:

NA.22

PubChem Substance ID:

24850386

eCl@ss:

32151902

UNSPSC Code:

12352100

EC Number:

213-280-6

MDL number:

MFCD00005596

Beilstein/REAXYS Number:

116525

Assay:

97%

Form:

solid

技术服务

需要帮助？我们经验丰富的科学家团队随时乐意为您服务。

让我们为您提供帮助

属性

Quality Level

100

assay

97%

form

solid

mp

226-230 °C (lit.)

SMILES string

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

Gene Information

human ... PLAU(5328)

说明

Application

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。

Still not finding the right product?

Explore all of our products under 2-氨基苯并咪唑

pictograms

GHS07

signalword

Warning

hcodes

H302

pcodes

P264 - P270 - P301 + P312 - P501

Hazard Classifications

Acute Tox. 4 Oral

存储类别

11 - Combustible Solids

wgk

WGK 3

ppe

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

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

没有发现合适的版本？

如果您需要特殊版本，可通过批号或批次号查找具体证书。

搜索COA

已有该产品？

在文件库中查找您最近购买产品的文档。

访问文档库

Programmed enzyme-mimic hydrolysis of a choline carbonate by a metal-free 2-aminobenzimidazole-based cavitand.

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

One-pot, two-step synthesis of imidazo[1,2-a]benzimidazoles via a multicomponent [4 + 1] cycloaddition reaction.

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

Removal of nonspecific binding proteins from cell and tissue extracts using 2-aminobenzimidazole-tethered affinity resin.

E Molnár et al.

Die Pharmazie, 66(9), 662-665 (2011-10-27)

Cellular drug target identification through affinity chromatography is often hindered by the quantity of nonspecific binders, such as cytoskeletal and heat shock proteins. Thus, we prepared a 2-aminobenzimidazole-tethered depletion resin designed for removal of these proteins, and tested it on

查看所有相关文献

全球贸易项目编号

货号	GTIN
171778-25G	04061838751195
171778-5G	04061838751201