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2,4,6-Trimethyl-1,3,5-dithiazine, also known as trimethyl-1,3,5-dithiazine, is a chemical compound characterized by its molecular formula C5H10N2S2. It features a cyclic disulfide with a six-membered ring structure, adorned with three methyl substituents attached to the nitrogen atoms. 2,4,6-Trimethyl-1,3,5-dithiazine is notably reactive and emits a strong odor, necessitating cautious handling and storage.

86241-90-9

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86241-90-9 Usage

Uses

Used in Organic Synthesis:
2,4,6-Trimethyl-1,3,5-dithiazine serves as a chemical intermediate in organic synthesis, playing a crucial role in the formation of various complex organic molecules. Its reactivity and structural features make it a valuable component in the synthesis of a wide range of compounds.
Used in Thiazine Derivatives Preparation:
As a reagent, 2,4,6-Trimethyl-1,3,5-dithiazine is utilized in the preparation of thiazine derivatives. These derivatives are important in various chemical and pharmaceutical applications, capitalizing on the compound's unique properties to create new and useful substances.
Used in Biological Activities and Therapeutic Applications Research:
2,4,6-Trimethyl-1,3,5-dithiazine has been the subject of research for its potential biological activities and therapeutic applications. While its strong reactivity and odor present challenges, scientists are exploring ways to harness its properties for beneficial uses in medicine and biology.
Used in Chemical Industry:
In the chemical industry, 2,4,6-Trimethyl-1,3,5-dithiazine is employed for its reactive nature, which allows it to participate in various chemical reactions and processes. Its use in this sector is diverse, spanning from the production of specialty chemicals to the development of new materials with unique properties.
Used in Pharmaceutical Development:
The pharmaceutical industry also explores 2,4,6-Trimethyl-1,3,5-dithiazine for its potential in drug development. Its unique structure and reactivity may contribute to the creation of new drugs or the enhancement of existing ones, particularly in the area of thiazine-based pharmaceuticals.
Given the compound's reactivity and strong odor, it is essential to handle and store 2,4,6-Trimethyl-1,3,5-dithiazine with the utmost care to ensure safety and effectiveness in its various applications.

Check Digit Verification of cas no

The CAS Registry Mumber 86241-90-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,6,2,4 and 1 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 86241-90:
(7*8)+(6*6)+(5*2)+(4*4)+(3*1)+(2*9)+(1*0)=139
139 % 10 = 9
So 86241-90-9 is a valid CAS Registry Number.
InChI:InChI=1S/C6H13NS2/c1-4-7-5(2)9-6(3)8-4/h4-7H,1-3H3

86241-90-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name thialdine

1.2 Other means of identification

Product number -
Other names Thialdin

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:86241-90-9 SDS

86241-90-9Relevant academic research and scientific papers

A Novel Method for the Generation of Thial S-Sulfides from 2,4,6-Trisubstituted 5,6-Dihydro-1,3,5-dithiazines

Takikawa, Yuji,Makabe, Takahiro,Hirose, Naoyuki,Hiratsuka, Takamichi,Takoh, Ryuji,Shimada, Kazuaki

, p. 1517 - 1520 (2007/10/02)

Treatment of 2,4,6-trisubstituted 5,6-dihydro-1,3,5-dithiazines with NCS or NBS afforded highly reactive thial S-sulfides, which underwent dimerization to give the corresponding 1,2,4,5-tetrathianes.The products were also selectively converted into naturally-occurring cyclic polysulfides, 1,2,4-trithiolanes and 1,2,3,5,6-pentathiepanes, by treatment with Ph3P, KCN, or Na2S4.

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