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6142-18-3

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6142-18-3 Usage

Description

2-Thiazolamine, N,N,4-trimethylis a chemical compound with the molecular formula C6H10N2S. It is a derivative of thiazole and contains a thioamide functional group. 2-Thiazolamine, N,N,4-trimethylis known for its potential applications in various fields, including organic synthesis, pharmaceuticals, agrochemicals, materials science, and catalysis.

Uses

Used in Organic Synthesis:
2-Thiazolamine, N,N,4-trimethylis used as a key intermediate in the synthesis of various organic compounds. Its unique structure and functional groups make it a versatile building block for the development of new molecules with potential applications in different industries.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 2-Thiazolamine, N,N,4-trimethylis used as a starting material for the production of various drugs. Its biological and pharmacological properties have been studied, and it has shown potential as a therapeutic agent for the treatment of certain diseases.
Used in Agrochemical Industry:
2-Thiazolamine, N,N,4-trimethylis also used in the agrochemical industry for the development of pesticides and other agricultural chemicals. Its unique chemical properties make it a valuable component in the creation of effective and environmentally friendly products.
Used in Materials Science:
In the field of materials science, 2-Thiazolamine, N,N,4-trimethylhas been investigated for its potential applications in the development of new materials with specific properties. Its ability to form stable complexes and interact with other molecules makes it a promising candidate for use in advanced materials.
Used in Catalysis:
2-Thiazolamine, N,N,4-trimethylhas been studied for its potential use as a catalyst in various chemical reactions. Its unique structure and functional groups allow it to facilitate specific reactions, making it a valuable tool in the field of catalysis.

Check Digit Verification of cas no

The CAS Registry Mumber 6142-18-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,1,4 and 2 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 6142-18:
(6*6)+(5*1)+(4*4)+(3*2)+(2*1)+(1*8)=73
73 % 10 = 3
So 6142-18-3 is a valid CAS Registry Number.

6142-18-3SDS

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 N,N,4-Trimethyl-1,3-thiazol-2-amine

1.2 Other means of identification

Product number -
Other names N,N,4-Trimethylthiazol-2-amine

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:6142-18-3 SDS

6142-18-3Relevant articles and documents

Reactions of 1-alkynyl thiocyanates with nucleophilic reagents. Synthesis of 2,4-disubstituted 1,3-thiazoles

Jong, R.L.P. de,Meijer, J.,Sukhai, R.S.,Bradsma, L.

, p. 310 - 313 (2007/10/02)

Reaction of 1-alkynyl thiocyanates RCC-S-CN (1) with alcohols, phenol or thiols or secondary aliphatic amines in the presence of anhydrous zinc chloride or boron trifluoride diethyl etherate gives mixtures of 2,4-disubstituted 1,3-thiazoles (2), thiocarbonyl compounds (3) (thiono esters, dithio esters or thioamides) and 2-alkylidene-1,3-dithioles (4).In all cases, the 1,3-thiazoles can be obtained in good yields if the proper reaction conditions are applied.Interaction between 1 and lithium dialkylamides LiNR'2 gives the compounds RCC-S-NR'2 (5) (attack on sulfur).With alkoxides R'O1-, the primary attack is on CN: the in termediacy alkynethiolate RCC-S1- subsequently reacts with the alkyl cyanate R'OCN to afford 1-alkynyl sulfides RCC-SR'(6)

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