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69015-51-6

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69015-51-6 Usage

Structure

Bicyclic heterocyclic compound with a chlorine atom and an ethyl group attached to the benzimidazole ring

Usage

Intermediate in the synthesis of various pharmaceuticals and organic compounds, suitable for the development of new drugs and related pharmaceutical research

Industrial and scientific applications

Suitable due to its structural properties

Check Digit Verification of cas no

The CAS Registry Mumber 69015-51-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,9,0,1 and 5 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 69015-51:
(7*6)+(6*9)+(5*0)+(4*1)+(3*5)+(2*5)+(1*1)=126
126 % 10 = 6
So 69015-51-6 is a valid CAS Registry Number.

69015-51-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-ethyl-5-chloro-1H-benzimidazole

1.2 Other means of identification

Product number -
Other names 1-Aethyl-5-chlor-1H-benzimidazol

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:69015-51-6 SDS

69015-51-6Downstream Products

69015-51-6Relevant articles and documents

Indole RSK inhibitors. Part 2: Optimization of cell potency and kinase selectivity

Kirrane, Thomas M.,Boyer, Stephen J.,Burke, Jennifer,Guo, Xin,Snow, Roger J.,Soleymanzadeh, Lida,Swinamer, Alan,Zhang, Yunlong,Madwed, Jeffery B.,Kashem, Mohammed,Kugler, Stanley,O'Neill, Margaret M.

, p. 738 - 742 (2012/03/11)

A series of inhibitors for the 90 kDa ribosomal S6 kinase (RSK) based on an 1-oxo-2,3,4,5-tetrahydro-1H-[1,4]diazepino[1,2-a]indole-8-carboxamide scaffold were optimized for cellular potency and kinase selectivity. This led to the identification of compound 24, BIX 02565, an attractive candidate for use in vitro and in vivo to explore the role of RSK as a target for the treatment heart failure.

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