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6-methyl-1,2,4-triazine-3,5(2H,4H)-dithione is an organic compound with the chemical formula C4H6N2S2. It is a derivative of the triazine ring system, which is a six-membered heterocyclic compound containing three nitrogen atoms. The molecule features a methyl group attached to the 6th position of the triazine ring and two dithione groups (sulfur-oxygen double bonds) at the 3rd and 5th positions. 6-methyl-1,2,4-triazine-3,5(2H,4H)-dithione is known for its potential applications in various chemical and pharmaceutical industries, as well as its use as a building block for the synthesis of other complex molecules. Due to its unique structure and properties, it has been the subject of research in the field of organic chemistry, with potential applications in areas such as agrochemicals and pharmaceuticals.

452-88-0

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452-88-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 452-88-0 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 4,5 and 2 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 452-88:
(5*4)+(4*5)+(3*2)+(2*8)+(1*8)=70
70 % 10 = 0
So 452-88-0 is a valid CAS Registry Number.

452-88-0SDS

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 6-methyl-2H-1,2,4-triazine-3,5-dithione

1.2 Other means of identification

Product number -
Other names 6-Methyl-3,5-dithioxo-1,2,4-triazin

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:452-88-0 SDS

452-88-0Downstream Products

452-88-0Relevant academic research and scientific papers

Deamination of some N-amino nitrogen heterocycles using Preyssler's anion

Heravi, Majid M.,Sadjadi, Sodeh,Hekmatshoar, Rahim,Oskooie, Hossein A.,Bamoharram, Fatemeh F.

, p. 107 - 110 (2008/09/20)

Some N-aminotriazines and -triazoles were treated with Preyssler's anion as catalyst in acetic acid to afford the corresponding deaminated triazines and triazoles. The reaction is suggested to proceed via formation of N-nitrosamines with subsequent N-NO b

Thiation of heterocycles using silica gel supported P2S5 under microwave irradiation in solventless system

Heravi,Rajabzadeh,Rahimizadeh,Bakavoli,Ghassemzadeh

, p. 2231 - 2234 (2007/10/03)

The efficient and environmentally friendly thiation of heterocycles using P2S5 under microwave irradiation in solvent free condition is described.

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