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Catalog Number:
17055
CAS Number:
40283-41-8
2-Aminothiazole-4-carboxylic acid
Purity:
≥ 99% (HPLC)
Synonym(s):
2-Amino-1,3-thiazole-4-carboxylic acid, 2-Amino-4-carboxythiazole
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Product Information

2-Aminothiazole-4-carboxylic acid is a versatile compound widely recognized for its applications in pharmaceuticals and agrochemicals. This heterocyclic compound features a thiazole ring, which contributes to its unique reactivity and biological activity. Researchers and industry professionals utilize 2-Aminothiazole-4-carboxylic acid as a building block in the synthesis of various bioactive molecules, including potential antimicrobial and anticancer agents. Its ability to act as a key intermediate in the development of novel therapeutic agents makes it invaluable in drug discovery and development processes.

In addition to its pharmaceutical relevance, 2-Aminothiazole-4-carboxylic acid is also employed in the formulation of agrochemicals, where it can enhance the efficacy of crop protection products. Its unique properties allow for the design of more effective herbicides and fungicides, contributing to improved agricultural productivity. With its diverse applications and potential for innovation, 2-Aminothiazole-4-carboxylic acid stands out as a crucial compound for researchers and professionals seeking to advance their work in medicinal chemistry and agricultural sciences.

Synonyms
2-Amino-1,3-thiazole-4-carboxylic acid, 2-Amino-4-carboxythiazole
CAS Number
40283-41-8
Purity
≥ 99% (HPLC)
Molecular Formula
C4H4N2O2S
Molecular Weight
144.15
MDL Number
MFCD00859429
PubChem ID
1501882
Melting Point
245 - 249 °C
Appearance
White to off-white solid
Conditions
Store at 0 - 8 °C
General Information
Synonyms
2-Amino-1,3-thiazole-4-carboxylic acid, 2-Amino-4-carboxythiazole
CAS Number
40283-41-8
Purity
≥ 99% (HPLC)
Molecular Formula
C4H4N2O2S
Molecular Weight
144.15
MDL Number
MFCD00859429
PubChem ID
1501882
Melting Point
245 - 249 °C
Appearance
White to off-white 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

2-Aminothiazole-4-carboxylic acid is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as a key intermediate in the synthesis of various pharmaceuticals, particularly in the development of antimicrobial agents and anti-inflammatory drugs.
  • Agricultural Chemistry: It is used in the formulation of agrochemicals, contributing to the development of effective pesticides and herbicides that enhance crop protection.
  • Biochemical Research: Researchers utilize this compound to study enzyme inhibition and metabolic pathways, aiding in the understanding of disease mechanisms and potential therapeutic targets.
  • Material Science: It plays a role in the synthesis of novel materials, including polymers and coatings, which exhibit unique properties beneficial for industrial applications.
  • Analytical Chemistry: This compound is employed as a standard in various analytical methods, facilitating the accurate quantification of related substances in complex mixtures.

Citations