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126006-77-7

126006-77-7

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  • Acetic acid,2-([1,1'-biphenyl]-4-yloxy)-, 2-[[(3-methylphenyl)amino]thioxomethyl]hydrazide

    Cas No: 126006-77-7

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126006-77-7 Usage

Chemical class

hydrazinecarbothioamide compound

Constituent groups

biphenyl-4-yloxyacetyl group, 3-methylphenyl group

Molecular weight

369.46 g/mol

Usage

pharmaceutical research and drug development

Basis for application

potential biological activities

Specific uses

may vary based on properties and interactions with other substances

Importance

valuable for further study and investigation

Check Digit Verification of cas no

The CAS Registry Mumber 126006-77-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,6,0,0 and 6 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 126006-77:
(8*1)+(7*2)+(6*6)+(5*0)+(4*0)+(3*6)+(2*7)+(1*7)=97
97 % 10 = 7
So 126006-77-7 is a valid CAS Registry Number.

126006-77-7SDS

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 1-(3-methylphenyl)-3-[[2-(4-phenylphenoxy)acetyl]amino]thiourea

1.2 Other means of identification

Product number -
Other names Acetic acid,((1,1'-biphenyl)-4-yloxy)-,2-(((3-methylphenyl)amino)thioxomethyl)hydrazide

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:126006-77-7 SDS

126006-77-7Downstream Products

126006-77-7Relevant articles and documents

Anti-inflammatory activity of substituted 1,3,4-oxadiazoles

Raman,Parmar,Salzman

, p. 999 - 1002 (2007/10/02)

Various 2-(4-biphenoxymethyl)-5-arylamino-1,3,4-oxadiazoles were synthesized by cyclization of the corresponding 1-(4-biphenoxyacetyl)-4-substituted thiosemicarbazides. These compounds were characterized by their elemental analyses and infrared, mass, and

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