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Catalog Number:
17528
CAS Number:
72030-87-6
Ester éthylique de l'acide 5-(4-nitrophényl)oxazole-4-carboxylique
Synonym(s):
5-(4-nitrophényl)-1,3-oxazole-4-carboxylate d'éthyle
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Product Information

5-(4-Nitrophenyl)oxazole-4-carboxylic acid ethyl ester is a versatile compound widely utilized in organic synthesis and pharmaceutical research. This compound features a unique oxazole ring structure, which enhances its reactivity and makes it an excellent candidate for various chemical transformations. Its nitrophenyl group contributes to its electronic properties, allowing for applications in the development of novel materials and intermediates in drug synthesis. Researchers have leveraged this compound in the synthesis of biologically active molecules, particularly in the fields of medicinal chemistry and agrochemicals, where it serves as a building block for the creation of complex structures.

The ethyl ester functionality not only improves the solubility of the compound but also facilitates its incorporation into various formulations, making it suitable for use in drug delivery systems. Its potential applications extend to the development of fluorescent probes and sensors, where its unique properties can be harnessed for detecting specific biological targets. With its robust profile and diverse applications, 5-(4-Nitrophenyl)oxazole-4-carboxylic acid ethyl ester stands out as a valuable tool for researchers and industry professionals seeking innovative solutions in chemical synthesis and material science.

Synonyms
5-(4-nitrophényl)-1,3-oxazole-4-carboxylate d'éthyle
CAS Number
72030-87-6
Molecular Formula
C12H10N2O5
Molecular Weight
262.22
MDL Number
MFCD02179429
PubChem ID
19614711
Conditions
Conserver à 0-8°C
General Information
Synonyms
5-(4-nitrophényl)-1,3-oxazole-4-carboxylate d'éthyle
CAS Number
72030-87-6
Molecular Formula
C12H10N2O5
Molecular Weight
262.22
MDL Number
MFCD02179429
PubChem ID
19614711
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

5-(4-Nitrophenyl)oxazole-4-carboxylic acid ethyl ester 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 inflammatory and cancer-related pathways.
  • Biochemical Research: It is used as a fluorescent probe in biochemical assays, helping researchers track cellular processes and interactions due to its unique optical properties.
  • Material Science: The compound finds applications in developing advanced materials, such as polymers and coatings, that require specific chemical properties for enhanced durability and performance.
  • Agricultural Chemistry: It is explored as a potential agrochemical, contributing to the development of new pesticides that are more effective and environmentally friendly.
  • Analytical Chemistry: This chemical is employed in analytical methods for detecting and quantifying specific biomolecules, providing researchers with reliable tools for studying complex biological systems.

Citations