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2,3,4,5-TETRAHYDRO-1,2,4-TRIAZINE-3,5-DITHIONE is an organic compound characterized by its heterocyclic structure, featuring a triazine ring and two thione functional groups. With the chemical formula C3H6N2S2, 2,3,4,5-TETRAHYDRO-1,2,4-TRIAZINE-3,5-DITHIONE is utilized in various chemical reactions and serves as a reagent in organic synthesis. Its unique structure endows it with the potential to function as a nucleophilic catalyst, facilitating the synthesis of a range of organic molecules. Moreover, it has garnered interest for its potential medicinal applications, particularly as an anti-cancer agent and in the treatment of neurodegenerative diseases, although further research is necessary to fully explore and exploit its capabilities.

461-90-5

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461-90-5 Usage

Uses

Used in Chemical Synthesis:
2,3,4,5-TETRAHYDRO-1,2,4-TRIAZINE-3,5-DITHIONE is used as a reagent in chemical synthesis for its ability to participate in various organic reactions, contributing to the formation of a wide array of molecules.
Used as a Nucleophilic Catalyst:
In the field of organic chemistry, 2,3,4,5-TETRAHYDRO-1,2,4-TRIAZINE-3,5-DITHIONE is utilized as a nucleophilic catalyst to enhance the rate of certain chemical reactions, thereby improving the efficiency of organic synthesis processes.
Used in Pharmaceutical Research:
2,3,4,5-TETRAHYDRO-1,2,4-TRIAZINE-3,5-DITHIONE is studied for its potential as an anti-cancer agent, with research indicating its possible role in the development of treatments for various types of cancer.
Used in Neurodegenerative Disease Treatment:
2,3,4,5-TETRAHYDRO-1,2,4-TRIAZINE-3,5-DITHIONE is also being investigated for its potential applications in the treatment of neurodegenerative diseases, suggesting that it may have therapeutic effects in conditions affecting the nervous system.

Check Digit Verification of cas no

The CAS Registry Mumber 461-90-5 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 4,6 and 1 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 461-90:
(5*4)+(4*6)+(3*1)+(2*9)+(1*0)=65
65 % 10 = 5
So 461-90-5 is a valid CAS Registry Number.

461-90-5SDS

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

1.2 Other means of identification

Product number -
Other names 2H-[1,2,4]triazine-3,5-dithione

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:461-90-5 SDS

461-90-5Downstream Products

461-90-5Relevant academic research and scientific papers

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.

Infrared spectra of 6-azathiouracils: An experimental matrix isolation and theoretical ab initio SCF/6-311G study

Lapinski, Leszek,Prusinowska, Dorota,Nowak, Maciej J.,Bretner, Maria,Felczak, Krzysztof,Maes, Guido,Adamowicz, Ludwik

, p. 645 - 659 (2007/10/03)

The infrared (IR) absorption spectra of 2-thio-6-azauracil, 4-thio-6-azauracil and 2,4-dithio-6-azauracil isolated in low-temperature Ar and N2 matrices are reported. These compounds have been found to exist in low-temperature matrices exclusively in the oxothione and dithione tautomeric forms. An assignment of the observed infrared bands is proposed on the basis of comparison of the experimental matrix spectra with the spectra calculated at the ab initio SCF/6-311G** level. The IR spectra of the title compounds are compared with the previously published IR spectra of matrix isolated 2-thiouracil, 4-thiouracil and 2,4-dithiouracil.

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