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Catalog Number:
44286
CAS Number:
14080-51-4
2-Aminothiophène-3-carboxamide
Purity:
≥ 98% (CG)
Hazmat
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Product Information

2-Aminothiophene-3-carboxamide is a versatile compound recognized for its significant applications in pharmaceuticals and organic synthesis. This compound features a thiophene ring, which enhances its electronic properties, making it valuable in the development of various bioactive molecules. Its unique structure allows for the potential synthesis of novel drugs, particularly in the fields of anti-inflammatory and antimicrobial agents. Researchers have utilized 2-Aminothiophene-3-carboxamide in the design of compounds that exhibit promising activity against a range of pathogens, showcasing its relevance in medicinal chemistry.

In addition to its pharmaceutical applications, 2-Aminothiophene-3-carboxamide serves as a key intermediate in the synthesis of agrochemicals and dyes, contributing to advancements in agricultural science and materials chemistry. Its ability to participate in diverse chemical reactions, such as coupling and cyclization, makes it an essential building block for chemists aiming to create complex molecular architectures. With its multifaceted uses and potential for innovation, 2-Aminothiophene-3-carboxamide stands out as a compound of interest for both researchers and industry professionals seeking to explore new frontiers in chemical applications.

CAS Number
14080-51-4
Purity
≥ 98% (CG)
Molecular Formula
C5H6N2OS
Molecular Weight
0
MDL Number
MFCD00706455
PubChem ID
699495
Melting Point
154 - 158 °C
Appearance
Poudre cristalline blanche à orange à verte
Conditions
Magasin chez RT
General Information
CAS Number
14080-51-4
Purity
≥ 98% (CG)
Molecular Formula
C5H6N2OS
Molecular Weight
0
MDL Number
MFCD00706455
PubChem ID
699495
Melting Point
154 - 158 °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
Oui
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

2-Aminothiophene-3-carboxamide is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as a building block in the synthesis of various pharmaceuticals, particularly those targeting neurological disorders, due to its ability to interact with specific receptors in the brain.
  • Agricultural Chemicals: It is employed in the formulation of agrochemicals, offering potential as a pesticide or herbicide, which helps in improving crop yield and protecting plants from pests.
  • Material Science: The compound is used in the development of conductive polymers and materials, enhancing the performance of electronic devices and sensors.
  • Analytical Chemistry: It acts as a reagent in analytical methods, aiding in the detection and quantification of various substances, which is crucial for quality control in manufacturing processes.
  • Biochemical Research: Researchers utilize this compound to study enzyme interactions and metabolic pathways, providing insights that can lead to innovative therapeutic strategies.

Citations