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Catalog Number:
17790
CAS Number:
14527-43-6
Ethyl 1,3-thiazole-4-carboxylate
Purity:
≥ 97% (HPLC)
Synonym(s):
Ethyl thiazole-4-carboxylate, 4-Thiazolecarboxylic acid ethyl ester
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Product Information

Ethyl 1,3-thiazole-4-carboxylate is a versatile compound known for its unique thiazole ring structure, which imparts significant chemical reactivity and stability. This compound is widely utilized in the synthesis of various pharmaceuticals and agrochemicals, making it an essential building block in medicinal chemistry. Its ability to act as a precursor in the development of bioactive molecules allows researchers to explore new therapeutic avenues, particularly in the fields of anti-inflammatory and antimicrobial agents.

In addition to its pharmaceutical applications, Ethyl 1,3-thiazole-4-carboxylate is also employed in the flavor and fragrance industry due to its distinctive aroma profile. This compound can enhance the sensory attributes of food products and perfumes, providing a competitive edge in formulation. Its favorable solubility and compatibility with various solvents further expand its utility across different sectors, including materials science and chemical research. With its broad range of applications and potential for innovation, Ethyl 1,3-thiazole-4-carboxylate is a valuable asset for professionals seeking to advance their projects.

Synonyms
Ethyl thiazole-4-carboxylate, 4-Thiazolecarboxylic acid ethyl ester
CAS Number
14527-43-6
Purity
≥ 97% (HPLC)
Molecular Formula
C6H7NO2S
Molecular Weight
157.19
MDL Number
MFCD03788566
PubChem ID
5003096
Appearance
Yellow solid
Conditions
Store at 0-8 °C
General Information
Synonyms
Ethyl thiazole-4-carboxylate, 4-Thiazolecarboxylic acid ethyl ester
CAS Number
14527-43-6
Purity
≥ 97% (HPLC)
Molecular Formula
C6H7NO2S
Molecular Weight
157.19
MDL Number
MFCD03788566
PubChem ID
5003096
Appearance
Yellow solid
Conditions
Store at 0-8 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Ethyl 1,3-thiazole-4-carboxylate is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as a key intermediate in the synthesis of various pharmaceuticals, particularly those targeting bacterial infections. Its unique thiazole ring enhances biological activity compared to similar compounds.
  • Agricultural Chemistry: It is used in the formulation of agrochemicals, including fungicides and herbicides, due to its effectiveness in controlling plant pathogens while being less toxic to beneficial organisms.
  • Flavor and Fragrance Industry: Ethyl 1,3-thiazole-4-carboxylate is employed as a flavoring agent in food products, imparting a unique taste profile that enhances the sensory experience of consumers.
  • Material Science: This compound is explored for its potential in creating novel materials, particularly in the development of polymers with enhanced properties, such as improved thermal stability and chemical resistance.
  • Biochemical Research: It is utilized in various biochemical assays and studies, helping researchers understand metabolic pathways and enzyme activities, thus facilitating advancements in biochemistry and molecular biology.

Citations