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Catalog Number:
25961
CAS Number:
910077-00-8
3-amino-5-(4-nitrophényl)thiophène-2-carboxylate d'éthyle
Purity:
≥ 98 % (HPLC)
Synonym(s):
Ester éthylique de l'acide 3-amino-5-(4-nitrophényl)-thiophène-2-carboxylique
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Product Information

Ethyl 3-amino-5-(4-nitrophenyl)thiophene-2-carboxylate is a versatile compound known for its significant applications in organic synthesis and pharmaceutical development. This compound features a unique thiophene ring structure, which enhances its reactivity and makes it an excellent candidate for various chemical transformations. Its nitrophenyl substituent contributes to its electronic properties, making it valuable in the design of novel materials and bioactive molecules. Researchers have utilized this compound in the synthesis of potential anti-cancer agents and other therapeutic compounds, showcasing its relevance in medicinal chemistry.

In addition to its pharmaceutical applications, Ethyl 3-amino-5-(4-nitrophenyl)thiophene-2-carboxylate is also explored in the field of organic electronics, particularly in the development of organic semiconductors and photovoltaic devices. Its ability to participate in electron transfer processes positions it as a promising material for enhancing the efficiency of electronic devices. With its unique properties and broad applicability, this compound stands out as a valuable resource for researchers and industry professionals looking to innovate in their respective fields.

Synonyms
Ester éthylique de l'acide 3-amino-5-(4-nitrophényl)-thiophène-2-carboxylique
CAS Number
910077-00-8
Purity
≥ 98 % (HPLC)
Molecular Formula
C13H12N2O4S
Molecular Weight
292.31
MDL Number
MFCD00428274
PubChem ID
13237883
Melting Point
170-178 ?C
Appearance
Poudre jaune foncé
Conditions
Conserver à 0-8°C
General Information
Synonyms
Ester éthylique de l'acide 3-amino-5-(4-nitrophényl)-thiophène-2-carboxylique
CAS Number
910077-00-8
Purity
≥ 98 % (HPLC)
Molecular Formula
C13H12N2O4S
Molecular Weight
292.31
MDL Number
MFCD00428274
PubChem ID
13237883
Melting Point
170-178 ?C
Appearance
Poudre jaune foncé
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

Ethyl 3-amino-5-(4-nitrophenyl)thiophene-2-carboxylate is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as a key intermediate in the synthesis of novel pharmaceuticals, particularly those targeting various diseases due to its unique chemical structure.
  • Organic Electronics: It is employed in the fabrication of organic electronic devices, such as organic light-emitting diodes (OLEDs), enhancing efficiency and performance due to its electron-accepting properties.
  • Biological Research: Researchers use this compound in studies related to enzyme inhibition and receptor binding, making it valuable for drug discovery and development.
  • Colorimetric Sensors: Its ability to undergo color changes in response to specific analytes makes it useful in creating sensors for detecting environmental pollutants or biological markers.
  • Material Science: The compound is explored for its potential in developing advanced materials with specific electrical and optical properties, which can be applied in various high-tech industries.

Citations