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216699-86-4

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216699-86-4 Usage

General Description

2-Chloro-6,7-dimethoxyquinoxaline is a chemical compound that falls under the family of quinoxalines - a class of organic compounds containing a quinoxaline moiety, a bicyclic heterocycle made up of a benzene ring fused to a pyrazine ring. This particular compound is known for its chloro group and methoxy groups attached to the quinoxaline structure. However, there is not much information available regarding its specific uses or properties. Often, quinoxalines are used in the development of various pharmaceuticals and therapeutic compounds, thus, 2-Chloro-6,7-dimethoxyquinoxaline could potentially have similar applications.

Check Digit Verification of cas no

The CAS Registry Mumber 216699-86-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,6,6,9 and 9 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 216699-86:
(8*2)+(7*1)+(6*6)+(5*6)+(4*9)+(3*9)+(2*8)+(1*6)=174
174 % 10 = 4
So 216699-86-4 is a valid CAS Registry Number.
InChI:InChI=1/C10H9ClN2O2/c1-14-8-3-6-7(4-9(8)15-2)13-10(11)5-12-6/h3-5H,1-2H3

216699-86-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Chloro-6,7-dimethoxyquinoxaline

1.2 Other means of identification

Product number -
Other names 2-chloro-6,7-dimethoxy-quinoxaline

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:216699-86-4 SDS

216699-86-4Downstream Products

216699-86-4Relevant articles and documents

Potent quinoxaline-based inhibitors of PDGF receptor tyrosine kinase activity. Part 2: The synthesis and biological activities of RPR127963 an orally bioavailable inhibitor

He, Wei,Myers, Michael R.,Hanney, Barbara,Spada, Alfred P.,Bilder, Glenda,Galzcinski, Helen,Amin, Dilip,Needle, Saul,Page, Ken,Jayyosi, Zaid,Perrone, Mark H.

, p. 3097 - 3100 (2003)

RPR127963 demonstrates an excellent pharmacokinetic profile in several species and was found to be efficacious in the prevention of restenosis in a Yucatan mini-pig model upon oral administration of 1-5 mg/kg. The in vitro selectivity profile and SAR of t

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