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650638-11-2

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650638-11-2 Usage

Structure

Benzimidazole derivative with a hydrazino group attached to the 4-position of the benzene ring

Industrial and pharmaceutical applications

Building block in the synthesis of various organic compounds, ligand in coordination chemistry, precursor to pharmaceuticals

Potential properties

Useful in biological research and drug development

Variation in properties and applications

May vary depending on specific uses and formulations

Check Digit Verification of cas no

The CAS Registry Mumber 650638-11-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,5,0,6,3 and 8 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 650638-11:
(8*6)+(7*5)+(6*0)+(5*6)+(4*3)+(3*8)+(2*1)+(1*1)=152
152 % 10 = 2
So 650638-11-2 is a valid CAS Registry Number.

650638-11-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1H-benzimidazol-4-ylhydrazine

1.2 Other means of identification

Product number -
Other names 1H-Benzimidazole,4-hydrazino

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:650638-11-2 SDS

650638-11-2Upstream product

650638-11-2Downstream Products

650638-11-2Relevant articles and documents

Novel GSK-3 inhibitors with improved cellular activity

Peat, Andrew J.,Garrido, Dulce,Boucheron, Joyce A.,Schweiker, Stephanie L.,Dickerson, Scott H.,Wilson, Jayme R.,Wang, Tony Y.,Thomson, Stephen A.

, p. 2127 - 2130 (2004)

A novel series of [1-(1H-benzimidazol-7-yl)-1H-pyrazolo[3,4-d]pyrimidin-4- yl] arylhydrazones was synthesized and shown to potently inhibit glycogen synthase kinase-3 (GSK-3). In light of detailed structure-activity relationships and structural knowledge of the GSK-3 binding pocket, a benzimidazole substituent was incorporated onto the pyrazolopyrimidine core resulting in improved potency over previous analogs. More importantly, these derivatives show low nanomolar efficacy for stimulating glycogen synthesis in vitro and therefore may be useful in the treatment of type 2 diabetes mellitus.

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