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4-TERT-BUTYL-2-METHYLTHIAZOLE, with the molecular formula C8H15NS, is a thiazole derivative characterized by its strong, nutty, and savory odor. It is recognized for its ability to impart a meaty or nutty flavor to food products and is also utilized as a fragrance ingredient in perfumes and personal care products. In addition to its applications in the food and cosmetic industries, it serves as a building block in the pharmaceutical industry for the synthesis of various drugs and pharmaceutical compounds.

15679-11-5

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15679-11-5 Usage

Uses

Used in Food Industry:
4-TERT-BUTYL-2-METHYLTHIAZOLE is used as a flavoring agent for its ability to impart a meaty or nutty flavor to food products, enhancing their taste and aroma.
Used in Cosmetics and Perfumery Industry:
4-TERT-BUTYL-2-METHYLTHIAZOLE is used as a fragrance ingredient in perfumes and personal care products, contributing to their distinct and appealing scents.
Used in Pharmaceutical Industry:
4-TERT-BUTYL-2-METHYLTHIAZOLE is used as a building block for the synthesis of various drugs and pharmaceutical compounds, playing a crucial role in the development of new medications.
Regulatory Considerations:
4-TERT-BUTYL-2-METHYLTHIAZOLE is considered safe for use in food and cosmetic products and is regulated by various government agencies to ensure its safety and proper usage.

Check Digit Verification of cas no

The CAS Registry Mumber 15679-11-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,6,7 and 9 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 15679-11:
(7*1)+(6*5)+(5*6)+(4*7)+(3*9)+(2*1)+(1*1)=125
125 % 10 = 5
So 15679-11-5 is a valid CAS Registry Number.
InChI:InChI=1/C8H13NS/c1-6-9-7(5-10-6)8(2,3)4/h5H,1-4H3

15679-11-5 Well-known Company Product Price

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  • Alfa Aesar

  • (A14148)  4-tert-Butyl-2-methylthiazole, 98%   

  • 15679-11-5

  • 5g

  • 381.0CNY

  • Detail
  • Alfa Aesar

  • (A14148)  4-tert-Butyl-2-methylthiazole, 98%   

  • 15679-11-5

  • 25g

  • 2083.0CNY

  • Detail

15679-11-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-TERT-BUTYL-2-METHYLTHIAZOLE

1.2 Other means of identification

Product number -
Other names 4-tert-Butyl-2-methylthiazole

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:15679-11-5 SDS

15679-11-5Relevant academic research and scientific papers

Synthesis of 2-imino-4-thiazolines, 2-imino-4-alkoxythiazolidines, thiazoles and 4-imidazolin-2-ones from α-halomethyl ketimines

De Kimpe, Norbert,De Cock, Wim,Keppens, Marian,De Smaele, Dirk,Meszaros, Andrea

, p. 1179 - 1183 (1996)

A variety of heterocycles, including 3,4-disubstituted-2-imino-4-thiazolines, 3,4-disubstituted-4-methoxy-2-iminothiazolidines, 2,4-disubstituted-thiazoles, 2-amino-4-substituted-thiazoles and 1,5-disubstituted-4-imidazolin-2-ones, were synthesized from α-chloromethyl and α-bromomethyl ketimines by condensation with potassium thiocyanate, thiourea, ammonium thiocyanate and potassium cyanate.

Synthesis of thiazoles and aminothiazoles from β-keto tosylates under supramolecular catalysis in the presence of β-cyclodextrin in water

Kumar, V. Pavan,Narender,Sridhar,Nageswar,Rao, K. Rama

, p. 4331 - 4336 (2008/03/13)

This is the first report on the supramolecular synthesis of thiazoles/aminothiazoles from β-keto tosylates and thioamide/thiourea in water in the presence of β-cyclodextrin in impressive yields. Formation of inclusion complexes was explained from 1H NMR studies. Copyright Taylor & Francis Group, LLC.

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