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Benzenepropanoic acid, b-(1H-1,2,4-triazol-3-ylthio)-, hydrazide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

827607-22-7

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827607-22-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 827607-22-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,2,7,6,0 and 7 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 827607-22:
(8*8)+(7*2)+(6*7)+(5*6)+(4*0)+(3*7)+(2*2)+(1*2)=177
177 % 10 = 7
So 827607-22-7 is a valid CAS Registry Number.

827607-22-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-Phenyl-3-(2H-[1,2,4]triazol-3-ylsulfanyl)-propionic acid hydrazide

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:827607-22-7 SDS

827607-22-7Downstream Products

827607-22-7Relevant academic research and scientific papers

Synthesis and transformations of 2-R-5-aryl-5,6-dihydro-7H-[1,2,4]- triazolo[5,1-b][1,3]thiazin-7-ones

Britsun,Esipenko,Kudryavtsev,Lozinskii

, p. 232 - 238 (2007/10/03)

A new procedure for preparation of 2-R-5-aryl-5,6-dihydro-7H-[1,2,4] triazolo[5,1-b][1,3]thiazin-7-ones by condensation of 5-R-1,2,4-triazole-3- thiones with 3-arylacryloyl chlorides was developed. The thiazine ring of the [1,2,4]triazolo[5,1-b][1,3]thiazin-7-ones is easily cleaved by treating with ammonia and hydrazine affording amides and hydrazides of 3-aryl-3-(1H-1,2,4- triazol-5-ylsulfanyl)propanoic acids. The latter react with isothiocyanates furnishing carbamoyl thiohydrazides of 3-aryl-3-(1H-1,2,4-triazol-5-ylsulfanyl) propanoic acids that in alkaline media undergo cyclization into 4-aryl-5-[2-(4H-1,2,4-triazol-5-ylsulfanyl)-2-phenylethyl]-2,4-dihydro-3H-1,2, 4-triazole-5-thiones.

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