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3176-53-2

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3176-53-2 Usage

Synthesis Reference(s)

The Journal of Organic Chemistry, 31, p. 3528, 1966 DOI: 10.1021/jo01349a014

Check Digit Verification of cas no

The CAS Registry Mumber 3176-53-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,1,7 and 6 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 3176-53:
(6*3)+(5*1)+(4*7)+(3*6)+(2*5)+(1*3)=82
82 % 10 = 2
So 3176-53-2 is a valid CAS Registry Number.

3176-53-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name CB-2959

1.2 Other means of identification

Product number -
Other names 3-phenyl-[1,2,4]triazolo[3,4-b][1,3,4]thiadiazol-6-ylamine

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:3176-53-2 SDS

3176-53-2Downstream Products

3176-53-2Relevant articles and documents

Synthesis, characterization and fungitoxicity of 3,4,6-triayl-striazolo [3,4-b]-1,3,4-thiadiazolo [1,3,5]-triazine-5-thiones

Mishra, Rakesh Mani

experimental part, p. 227 - 232 (2012/01/07)

In the present work 3,4,6-triayl-s-triazolo [3,4-b]-1,3,4-thiadiazolo [1,3,50-triazine-5-thiones (IVan) were synehsized by 4+2 cycloaddition of 6-arylidine amino-3-aryl-s-triazolo [3,4-b]-1,3,4-thiadiazoles (IIIa-n) are arylisothiocynate in dry tolune as solvent. 6-Arylidine amino-3-aryl-s-triazolo [3,4-b]-1,3,4-thiadiazoles (IIIa-n) were prepared from aromatic aldehyde refluxing in absolute ethanol with 6-amino-3-aryl-s-triazole [3,4-b]-1,3,4-thiadiazoles (IIa-g), which are prepared from 3-aryl, 4-amino-5-mercaptos-triazole (Ia-g) by treating it with cyanogen bromide in ethanol. Starting material 3-aryl, 4-amino-5-mercapto-s-triazoles (Ia-g) wre prepred in excellent yield following the method of Ried and Heindel1. The reaction sequence leading to the formation of titled compounds are given in the scheme 1. All the synthesized fourteen titled compounds were well characterized by their analytical and spectral data. Fungitoxicity of titled compounds (IVa-n) have been evaluated against two fungal species i.e. Helminthosporium orayzee and Alternaria solanai.

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