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Catalog Number:
18190
CAS Number:
23012-14-8
Ester éthylique de l'acide oxazole-4-carboxylique
Purity:
≥ 98 % (HPLC)
Synonym(s):
4-oxazolecarboxylate d'éthyle, 1,3-oxazole-4-carboxylate d'éthyle
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Product Information

Oxazole-4-carboxylic acid ethyl ester is a versatile compound recognized for its unique oxazole ring structure, which imparts significant chemical reactivity and stability. This compound is widely utilized in the synthesis of pharmaceuticals and agrochemicals, serving as a key intermediate in the development of various bioactive molecules. Its ability to participate in diverse chemical reactions makes it an essential building block in organic synthesis, particularly in the creation of heterocyclic compounds that are crucial in medicinal chemistry.

In addition to its applications in drug development, Oxazole-4-carboxylic acid ethyl ester is also employed in the formulation of specialty chemicals and materials, enhancing properties such as solubility and stability. Researchers and industry professionals appreciate its efficiency in streamlining synthetic pathways, thereby reducing production costs and time. With its favorable characteristics and broad applicability, this compound holds significant potential for innovation in various chemical industries.

Synonyms
4-oxazolecarboxylate d'éthyle, 1,3-oxazole-4-carboxylate d'éthyle
CAS Number
23012-14-8
Purity
≥ 98 % (HPLC)
Molecular Formula
C 6 H 7 NO 3
Molecular Weight
141.13
MDL Number
MFCD04114940
PubChem ID
2763217
Appearance
Solide blanc à jaune pâle
Conditions
Conserver à 0-8 °C
General Information
Synonyms
4-oxazolecarboxylate d'éthyle, 1,3-oxazole-4-carboxylate d'éthyle
CAS Number
23012-14-8
Purity
≥ 98 % (HPLC)
Molecular Formula
C 6 H 7 NO 3
Molecular Weight
141.13
MDL Number
MFCD04114940
PubChem ID
2763217
Appearance
Solide blanc à jaune pâle
Conditions
Conserver à 0-8 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

Oxazole-4-carboxylic acid ethyl ester is widely utilized in research focused on

  • Synthetic Chemistry: This compound serves as a versatile building block in the synthesis of various pharmaceuticals and agrochemicals, enabling the development of new drugs and crop protection agents.
  • Biological Research: It is used in studies investigating the biological activity of oxazole derivatives, which can lead to the discovery of new therapeutic agents with potential anti-inflammatory or antimicrobial properties.
  • Material Science: The compound is explored in the creation of novel polymers and materials, enhancing properties such as thermal stability and mechanical strength, which are crucial for industrial applications.
  • Analytical Chemistry: Oxazole-4-carboxylic acid ethyl ester is employed as a standard in chromatographic techniques, aiding in the accurate quantification of related compounds in complex mixtures.
  • Food Industry: Its derivatives are investigated for use as flavoring agents or preservatives, providing natural alternatives that can enhance food safety and quality.

Citations