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13139-47-4

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13139-47-4 Usage

General Description

2-acetylthiazole-4-carboxylic acid is a chemical compound with a molecular formula of C8H7NO3S. It is a derivative of thiazole and is commonly used as a flavoring agent in the food industry due to its nutty, popcorn-like aroma. It is also used in the fragrance industry to add a warm, earthy scent to perfumes and other scented products. 2-acetylthiazole-4-carboxylic acid is known for enhancing the overall flavor and aroma of various food and beverage products. Additionally, it can be used as a building block in the synthesis of other pharmaceutical and chemical compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 13139-47-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,1,3 and 9 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 13139-47:
(7*1)+(6*3)+(5*1)+(4*3)+(3*9)+(2*4)+(1*7)=84
84 % 10 = 4
So 13139-47-4 is a valid CAS Registry Number.
InChI:InChI=1/C6H5NO3S/c1-3(8)5-7-4(2-11-5)6(9)10/h2H,1H3,(H,9,10)

13139-47-4SDS

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 2-acetyl-1,3-thiazole-4-carboxylic acid

1.2 Other means of identification

Product number -
Other names 2-Acetylthiazole-4-carboxylicacid

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:13139-47-4 SDS

13139-47-4Relevant articles and documents

Synthesis of Triarylpyridines in Thiopeptide Antibiotics by Using a C-H Arylation/Ring-Transformation Strategy

Amaike, Kazuma,Itami, Kenichiro,Yamaguchi, Junichiro

, p. 4384 - 4388 (2016)

We have described a C-H arylation/ring-transformation strategy for the synthesis of triarylpyridines, which form the core structure of thiopeptide antibiotics. This synthetic method readily gave 2,3,6-triarylpyridines in a regioselective manner by a two-p

Total synthesis of the thiopeptide antibiotic amythiamicin D

Hughes, Rachael A.,Thompson, Stewart P.,Alcaraz, Lilian,Moody, Christopher J.

, p. 15644 - 15651 (2007/10/03)

The thiopeptide (or thiostrepton) antibiotics are a class of sulfur containing highly modified cyclic peptides with interesting biological properties, including reported activity against MRSA and malaria. Described herein is the total synthesis of the thi

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