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15729-76-7

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15729-76-7 Usage

General Description

2,5-Diethylthiazole is a chemical compound that belongs to the family of thiazoles, which are aromatic compounds containing a five-member ring made up of three carbon atoms, one nitrogen atom, and one sulfur atom. 2,5-Diethylthiazole is characterized by its two ethyl groups located at the second and fifth carbon atoms in the ring. It is commonly used in the flavor and fragrance industries because of its unique nutty, corn-like aroma. Like many thiazoles, this chemical has important applications in the field of organic synthesis, serving as a key building block in the creation of more complex organic molecules.

Check Digit Verification of cas no

The CAS Registry Mumber 15729-76-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,7,2 and 9 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 15729-76:
(7*1)+(6*5)+(5*7)+(4*2)+(3*9)+(2*7)+(1*6)=127
127 % 10 = 7
So 15729-76-7 is a valid CAS Registry Number.
InChI:InChI=1/C7H11NS/c1-3-6-5-8-7(4-2)9-6/h5H,3-4H2,1-2H3

15729-76-7SDS

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 2,5-diethyl-1,3-thiazole

1.2 Other means of identification

Product number -
Other names EINECS 239-823-7

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only. Food additives -> Flavoring Agents
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:15729-76-7 SDS

15729-76-7Downstream Products

15729-76-7Relevant articles and documents

Synthesis of 2,4-diacetylthiazole and 2,5-diacetylthiazole

Aitken, Kati M.,Aitken, R. Alan

, p. 4384 - 4386 (2008)

Compounds 2,4-diacetylthiazole 5 and 2,5-diacetylthiazole 6, of interest for their flavour and aroma properties, have been prepared for the first time by tetrabromination and silver nitrate treatment of the corresponding diethylthiazoles.

Preparation of α-methyl-substituted dialkyl ketones by alkaline opening of 1,2-dialkyl-substituted cyclopropanols

Savchenko

, p. 1182 - 1183 (2007/10/03)

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α-Methylation of ketones via manganese-enolates: Absence of undesired polyalkylation

Reetz, Manfred T.,Haning, Helmut

, p. 7395 - 7398 (2007/10/02)

The transmetalation of ketone lithium-enolates using MnBr2 generates manganese-enolates which react with CH3I to provide α-methylated ketones with essentially no undesired polyalkylated byproducts.

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