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2-(Methylthio)-4-(tributylstannyl)thiazole is a chemical compound characterized by a thiazole ring with a methylthio group at the 2-position and a tributylstannyl group at the 4-position. Thiazoles are heterocyclic compounds commonly found in pharmaceuticals and agrochemicals. The methylthio group consists of a sulfur atom bonded to a methyl group, while the tributylstannyl group features a tin atom bonded to four butyl groups. These functional groups provide reactive sites for further chemical reactions, making 2-(Methylthio)-4-(tributylstannyl)thiazole a versatile compound in organic synthesis, materials chemistry, and potentially in biological applications. However, due to the presence of tin, safety precautions are necessary when handling this chemical.

446286-06-2

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446286-06-2 Usage

Uses

Used in Organic Synthesis:
2-(Methylthio)-4-(tributylstannyl)thiazole is used as a synthetic intermediate for the preparation of various organic compounds. Its reactive functional groups facilitate the formation of new chemical bonds and the synthesis of complex molecules.
Used in Materials Chemistry:
In materials chemistry, 2-(Methylthio)-4-(tributylstannyl)thiazole is used as a building block for the development of new materials with specific properties. Its unique structure and functional groups can contribute to the creation of materials with tailored characteristics for various applications.
Used in Pharmaceutical Industry:
2-(Methylthio)-4-(tributylstannyl)thiazole is used as a potential pharmaceutical agent due to its presence in heterocyclic compounds, which are often found in drug molecules. Its unique structure and functional groups may contribute to the development of new drugs with novel therapeutic properties.
Used in Agrochemical Industry:
In the agrochemical industry, 2-(Methylthio)-4-(tributylstannyl)thiazole may be used as a precursor for the synthesis of agrochemicals, such as pesticides and herbicides. Its reactive functional groups can be utilized to create compounds with specific biological activities against pests and weeds.
Note: The specific applications and industries mentioned above are hypothetical and based on the general properties of the compound. Further research and development would be required to determine the actual uses and potential of 2-(Methylthio)-4-(tributylstannyl)thiazole in these areas.

Check Digit Verification of cas no

The CAS Registry Mumber 446286-06-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,4,6,2,8 and 6 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 446286-06:
(8*4)+(7*4)+(6*6)+(5*2)+(4*8)+(3*6)+(2*0)+(1*6)=162
162 % 10 = 2
So 446286-06-2 is a valid CAS Registry Number.
InChI:InChI=1/C4H4NS2.3C4H9.Sn/c1-6-4-5-2-3-7-4;3*1-3-4-2;/h3H,1H3;3*1,3-4H2,2H3;/rC16H31NS2Sn/c1-5-8-11-20(12-9-6-2,13-10-7-3)15-14-19-16(17-15)18-4/h14H,5-13H2,1-4H3

446286-06-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(Methylthio)-4-(tributylstannyl)thiazole

1.2 Other means of identification

Product number -
Other names tributyl-(2-methylsulfanyl-1,3-thiazol-4-yl)stannane

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:446286-06-2 SDS

446286-06-2Upstream product

446286-06-2Downstream Products

446286-06-2Relevant academic research and scientific papers

Composition and antiviral activity of substituted azaindoleoxoacetic piperazine derivatives

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Page 108, (2008/06/13)

This invention provides compounds having drug and bio-affecting properties, their pharmaceutical compositions and method of use. In particular, the invention is concerned with azaindoleoxoacetyl piperazine derivatives. These compounds possess unique antiviral activity, whether used alone or in combination with other antivirals, antiinfectives, immunomodulators or HIV entry inhibitors. More particularly, the present invention relates to the treatment of HIV and AIDS.

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