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77331-28-3

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77331-28-3 Usage

Class

1,2,4-triazoles

Uses

a. Synthesis of pharmaceuticals and agrochemicals
b. Catalyst or reagent in various organic reactions
c. Potential applications in material science and medicinal chemistry

Physical state

Yellow crystalline solid

Molecular weight

325.84 g/mol

Biological and pharmacological properties

May have properties of interest for further research and development

Check Digit Verification of cas no

The CAS Registry Mumber 77331-28-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,7,3,3 and 1 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 77331-28:
(7*7)+(6*7)+(5*3)+(4*3)+(3*1)+(2*2)+(1*8)=133
133 % 10 = 3
So 77331-28-3 is a valid CAS Registry Number.

77331-28-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-methylthio-1,4-diphenyl-1,2,4-triazolium chloride

1.2 Other means of identification

Product number -
Other names -

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:77331-28-3 SDS

77331-28-3Relevant articles and documents

STABLE CARBON-YLIDES

Doleschall, Gabor,Seres, Peter

, p. 209 - 216 (2007/10/02)

5-Acylmethylene-1,2,4-triazolium salts were synthesized and converted to stable anhydrobases by aqueous alkali.The close analogy of their spectra with those of phosphorus-ylides and their reactions suggest that the anhydrobases may be regarded as carbon-ylides. α,β-Unsaturated aldehydes were synthesized in moderate yield by selective reduction of the salts folloved by acid hydrolysis.

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