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Catalog Number:
43076
CAS Number:
90924-54-2
5-(thiophén-2-yl)isoxazole-3-carboxylate d'éthyle
Purity:
≥ 98% (CG)
Synonym(s):
Ester éthylique de l'acide 5-(thiophén-2-yl)isoxazole-3-carboxylique
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Product Information

Ethyl 5-(thiophen-2-yl)isoxazole-3-carboxylate is a versatile compound known for its unique structural features, making it valuable in various fields, particularly in medicinal chemistry and organic synthesis. This compound exhibits significant potential as a building block for the development of novel pharmaceuticals, especially in the search for new anti-inflammatory and anti-cancer agents. Its thiophene moiety enhances its biological activity, allowing researchers to explore its efficacy in drug design and development.

In addition to its pharmaceutical applications, Ethyl 5-(thiophen-2-yl)isoxazole-3-carboxylate can be utilized in the synthesis of agrochemicals, providing a pathway for the creation of effective pesticides and herbicides. Its stability and reactivity make it an attractive option for chemists looking to innovate in the field of crop protection. With its promising applications and unique properties, this compound stands out as a key ingredient for researchers and industry professionals aiming to advance their projects in drug discovery and agricultural chemistry.

Synonyms
Ester éthylique de l'acide 5-(thiophén-2-yl)isoxazole-3-carboxylique
CAS Number
90924-54-2
Purity
≥ 98% (CG)
Molecular Formula
C 10 H 9 NO 3 S
Molecular Weight
223.25
MDL Number
MFCD02090509
PubChem ID
2745138
Melting Point
51 - 55 °C
Appearance
Poudre cristalline blanche à orange à verte
Conditions
Magasin chez RT
General Information
Synonyms
Ester éthylique de l'acide 5-(thiophén-2-yl)isoxazole-3-carboxylique
CAS Number
90924-54-2
Purity
≥ 98% (CG)
Molecular Formula
C 10 H 9 NO 3 S
Molecular Weight
223.25
MDL Number
MFCD02090509
PubChem ID
2745138
Melting Point
51 - 55 °C
Appearance
Poudre cristalline blanche à orange à verte
Conditions
Magasin chez RT
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

Ethyl 5-(thiophen-2-yl)isoxazole-3-carboxylate is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as a building block in the synthesis of novel drugs, particularly in the development of anti-inflammatory and analgesic agents, due to its unique structure that can interact with biological targets effectively.
  • Agricultural Chemistry: It is used in the formulation of agrochemicals, enhancing the efficacy of pesticides and herbicides. Its ability to improve the bioavailability of active ingredients makes it valuable in crop protection.
  • Material Science: The compound is explored for its potential in creating advanced materials, such as polymers and coatings, that require specific thermal and mechanical properties, providing durability and resistance to environmental factors.
  • Organic Synthesis: It acts as an important intermediate in organic synthesis, allowing chemists to create complex molecules with high specificity and yield, which is crucial for various industrial applications.
  • Research in Organic Electronics: The compound is investigated for its role in organic electronic devices, such as organic light-emitting diodes (OLEDs) and organic photovoltaics, where its electronic properties can enhance device performance.

Citations