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5-(2-chlorophenyl)-3-{[(2-chlorophenyl)amino]methyl}-1,3,4-oxadiazole-2(3H)-thione is a complex organic compound with the molecular formula C14H9Cl2N3OS. It features a 1,3,4-oxadiazole-2(3H)-thione core structure, which is a five-membered heterocyclic ring containing oxygen, sulfur, and nitrogen atoms. The compound has two chlorophenyl groups attached to the oxadiazole core, with one being directly connected to the 5-position and the other forming an aminomethyl linkage at the 3-position. This molecule is characterized by its potential applications in pharmaceuticals and agrochemicals, as well as its unique chemical properties due to the presence of chlorine atoms and the heterocyclic structure.

6074-92-6

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6074-92-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6074-92-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,0,7 and 4 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 6074-92:
(6*6)+(5*0)+(4*7)+(3*4)+(2*9)+(1*2)=96
96 % 10 = 6
So 6074-92-6 is a valid CAS Registry Number.

6074-92-6SDS

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 3-[(2-chloroanilino)methyl]-5-(2-chlorophenyl)-1,3,4-oxadiazole-2-thione

1.2 Other means of identification

Product number -
Other names 5-(2-chlorophenyl)-3-{[(2-chlorophenyl)amino]methyl}-1,3,4-oxadiazole-2(3H)-thione

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 -
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More Details:6074-92-6 SDS

6074-92-6Downstream Products

6074-92-6Relevant academic research and scientific papers

131. Regioselective Functionalisation of N,N-Diethyl-1,6-methanoannulene-2-carboxamides

Neidlein, Richard,Wirth, Wolfgang

, p. 1263 - 1270 (1986)

Lithiation of N,N-diethyl-1,6-methanoannulene-2-carboxamide with BuLi followed by quenching with different electrophiles yields 2,10-disubstituted-1,6-methanoannulenes.

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