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55686-93-6

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55686-93-6 Usage

Synthesis Reference(s)

Journal of Medicinal Chemistry, 44, p. 1758, 2001 DOI: 10.1021/jm0005149

Check Digit Verification of cas no

The CAS Registry Mumber 55686-93-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,5,6,8 and 6 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 55686-93:
(7*5)+(6*5)+(5*6)+(4*8)+(3*6)+(2*9)+(1*3)=166
166 % 10 = 6
So 55686-93-6 is a valid CAS Registry Number.
InChI:InChI=1/C9H7ClN2O/c1-13-6-2-3-7-8(4-6)12-9(10)5-11-7/h2-5H,1H3

55686-93-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Chloro-7-methoxyquinoxaline

1.2 Other means of identification

Product number -
Other names W6957

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:55686-93-6 SDS

55686-93-6Relevant articles and documents

Hepatitis C virus inhibitors

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Page/Page column 613; 614, (2017/01/23)

Hepatitis C virus inhibitors having the general formula (I) are disclosed. Compositions comprising the compounds and methods for using the compounds to inhibit HCV are also disclosed.

Hepatitis C Virus Inhibitors

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Page/Page column, (2013/05/21)

Hepatitis C virus inhibitors having the general formula (I) are disclosed. Compositions comprising the compounds and methods for using the compounds to inhibit HCV are also disclosed.

HETEROARYL DERIVATIVES AS OREXIN RECEPTOR ANTAGONISTS

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Page/Page column 54-55, (2009/07/10)

The present invention relates to compounds of formula wherein Ar, Het, R1 and n are as defined herein and to pharmaceutically suitable acid addition salts, optically pure enantiomers, racemates or diastereomeric mixtures thereof. Compounds of formula I are orexin receptor antagonists and are useful in the treatment of sleep apnea, narcolepsy, insomnia, parasomnia, jet lag syndrome, circadian rhythms disorder and sleep disorders associated with neurological diseases.

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