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.

InChI:InChI=1/C6H5NO3S/c1-3(8)5-7-4(2-11-5)6(9)10/h2H,1H3,(H,9,10)

Upstream product

• 1087345-72-9 2-(1-amino-ethyl)-thiazole-4-carboxylic acid; monohydrochloride 
• 160060-21-9 2-acetylthiazol-4-carboxylic acid ethyl ester 
• 73956-16-8 ethyl 2-(diethoxymethyl)-1,3-thiazole-4-carboxylate 
• 73956-17-9 ethyl 2-formyl-1,3-thiazole-4-carboxylate 
• 1372541-86-0 ethyl 2-(diethoxymethyl)-2-thiazoline-4-carboxylate 
• 161891-80-1 (+/-)-4-ethoxycarbonyl-2-(1-hydroxyethyl)thiazole 

Downstream Products

• 156620-46-1 amythiamicin D 
• 706785-52-6 benzyl 2-(1-acetylaminoethenyl)thiazole-4-carboxylate 
• 870820-77-2 benzyl 2-(1-hydroxyiminoethyl)thiazole-4-carboxylate 
• 706785-50-4 benzyl 2-acetylthiazole-4-carboxylate 

Relevant academic research and scientific papers

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

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

Easy access to 2-alkyl and 2-arylthiazolines using a modified heteropolyacid catalysis: Application to the synthesis of bacillamide A

A straightforward access to 2-alkyl and 2-arylthiazolines by condensation of-aminothiols on nitriles, catalyzed by phosphotungstic acid (2%) under microwave irradiation, is described. This method has been directly applied to a short and efficient synthesi

Total synthesis of the thiopeptide antibiotic amythiamicin D

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

Total synthesis of the thiopeptide amythiamicin D.

The first total synthesis of the thiopeptide antibiotic amythiamicin D is described.