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2H-1,2,4-Triazepine, 2-methyl-3,5-bis(methylthio)-7-phenylis a heterocyclic organic compound with a molecular formula of C17H20N2S2. It features a seven-membered ring with three nitrogen atoms and one sulfur atom. 2H-1,2,4-Triazepine, 2-methyl-3,5-bis(methylthio)-7-phenylis of interest in pharmaceutical and chemical research due to its potential medicinal and industrial applications. Its specific properties and potential uses are still being studied and evaluated.

177534-54-2

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177534-54-2 Usage

Uses

Used in Pharmaceutical Research:
2H-1,2,4-Triazepine, 2-methyl-3,5-bis(methylthio)-7-phenylis used as a chemical intermediate for the development of new pharmaceutical compounds. Its unique structure and properties make it a promising candidate for the creation of novel drugs with potential therapeutic applications.
Used in Chemical Research:
In the field of chemical research, 2H-1,2,4-Triazepine, 2-methyl-3,5-bis(methylthio)-7-phenylis utilized for studying the synthesis and reactions of heterocyclic compounds. Its reactivity and stability contribute to the advancement of knowledge in organic chemistry and the development of new chemical processes and materials.

Check Digit Verification of cas no

The CAS Registry Mumber 177534-54-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,7,5,3 and 4 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 177534-54:
(8*1)+(7*7)+(6*7)+(5*5)+(4*3)+(3*4)+(2*5)+(1*4)=162
162 % 10 = 2
So 177534-54-2 is a valid CAS Registry Number.

177534-54-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-methyl-3,5-bis(methylsulfanyl)-7-phenyl-1,2,4-triazepine

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 -
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More Details:177534-54-2 SDS

177534-54-2Downstream Products

177534-54-2Relevant academic research and scientific papers

Regioselective synthesis of new biheterocyclic triazepines

Ait Itto,Hasnaoui,Riahi,Lavergne

, p. 2087 - 2090 (2007/10/03)

Condensation of dihaloalkanes to 1,2,4-triazepine 1a in the Phase Transfer Catalysis (P.T.C.) conditions provides efficient and facile access to biheterocyclic triazepines with high regioselectivity. In the same conditions, the triazepinone 1b has been found to degradate after alkylation to give pyrazoles.

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