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Benzenamine, 2-(1,2,3-thiadiazol-4-yl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

286955-98-4

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286955-98-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 286955-98-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,8,6,9,5 and 5 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 286955-98:
(8*2)+(7*8)+(6*6)+(5*9)+(4*5)+(3*5)+(2*9)+(1*8)=214
214 % 10 = 4
So 286955-98-4 is a valid CAS Registry Number.

286955-98-4SDS

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 4-(2-aminophenyl)-1,2,3-thiadiazole

1.2 Other means of identification

Product number -
Other names 2-[1,2,3]Thiadiazol-4-yl-phenylamine

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:286955-98-4 SDS

286955-98-4Downstream Products

286955-98-4Relevant academic research and scientific papers

Nucleophilic intramolecular cyclization reactions of alkynechalcogenolates

Abramov,Dehaen,D'Hooge,Petrov,Smeets,Toppet,Voets

, p. 3933 - 3940 (2007/10/03)

2-(ortho-Hydroxyphenyl)-alkynethiolates and -selenolates, obtained through base catalyzed ring cleavage of 4-(ortho-hydroxyphenyl)-1,2,3- thiadiazoles and -1,2,3-selenadiazoles, smoothly transform into 2- benzofuranthiolates and -selenolates. These reactive intermediates can be alkylated in high yield. This reaction sequence could be applied to the synthesis of electron rich thiacrown ethers. The 2-(ortho-aminophenyl)- alkynethiolate analogously forms 2-methylsulfanylindole. (C) 2000 Elsevier Science Ltd.

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