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Catalog Number:
44218
CAS Number:
4815-34-3
2-amino-5-phénylthiophène-3-carboxylate d'éthyle
Purity:
≥ 98% (CG)
Synonym(s):
Ester éthylique de l'acide 2-amino-5-phénylthiophène-3-carboxylique
Documents
$42.16 /200 mg
Taille
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Product Information

Ethyl 2-amino-5-phenylthiophene-3-carboxylate is a versatile compound known for its significant role in organic synthesis and medicinal chemistry. This compound features a unique thiophene ring structure, which enhances its reactivity and makes it a valuable intermediate in the production of various pharmaceuticals and agrochemicals. Its amino and carboxylate functional groups allow for diverse chemical modifications, enabling researchers to tailor its properties for specific applications.

In the pharmaceutical industry, Ethyl 2-amino-5-phenylthiophene-3-carboxylate has been explored for its potential as a building block in the synthesis of bioactive molecules, including anti-inflammatory and antimicrobial agents. Its ability to participate in various coupling reactions makes it an essential component in the development of novel therapeutic compounds. Additionally, its stability and solubility characteristics contribute to its suitability for use in various formulations, enhancing its appeal to researchers and industry professionals alike.

Synonyms
Ester éthylique de l'acide 2-amino-5-phénylthiophène-3-carboxylique
CAS Number
4815-34-3
Purity
≥ 98% (CG)
Molecular Formula
C 13 H 13 NO 2 S
Molecular Weight
247.31
MDL Number
MFCD01829801
PubChem ID
638860
Melting Point
122 - 126 °C
Appearance
Poudre cristalline blanche à jaune à verte
Conditions
Magasin chez RT
General Information
Synonyms
Ester éthylique de l'acide 2-amino-5-phénylthiophène-3-carboxylique
CAS Number
4815-34-3
Purity
≥ 98% (CG)
Molecular Formula
C 13 H 13 NO 2 S
Molecular Weight
247.31
MDL Number
MFCD01829801
PubChem ID
638860
Melting Point
122 - 126 °C
Appearance
Poudre cristalline blanche à jaune 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 2-amino-5-phenylthiophene-3-carboxylate 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 drugs targeting neurological disorders.
  • Organic Synthesis: It is used in organic chemistry for creating complex molecules, offering a versatile building block for researchers in the field of medicinal chemistry.
  • Material Science: The compound is explored for its potential applications in creating conductive polymers, which are essential in the development of electronic devices.
  • Biological Research: Ethyl 2-amino-5-phenylthiophene-3-carboxylate is investigated for its biological activity, providing insights into its effects on cellular processes and potential therapeutic benefits.
  • Analytical Chemistry: It is utilized as a standard reference material in analytical methods, helping researchers ensure accuracy and reliability in their experimental results.

Citations