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Catalog Number:
44274
CAS Number:
43088-42-2
Ethyl 2-amino-4-methylthiophene-3-carboxylate
Purity:
≥ 98% (GC)
Synonym(s):
2-Amino-4-methylthiophene-3-carboxylic acid ethyl ester
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Product Information

Ethyl 2-amino-4-methylthiophene-3-carboxylate is a versatile compound recognized for its significant applications in pharmaceutical and chemical research. This compound features a unique thiophene ring structure, which enhances its reactivity and makes it an excellent candidate for the synthesis of various biologically active molecules. Its amino and carboxylate functional groups provide opportunities for further chemical modifications, allowing researchers to explore a wide range of derivatives with potential therapeutic benefits.

In the pharmaceutical industry, Ethyl 2-amino-4-methylthiophene-3-carboxylate can serve as a building block in the development of novel drugs, particularly those targeting neurological and metabolic disorders. Its ability to participate in diverse chemical reactions, such as nucleophilic substitutions and coupling reactions, makes it a valuable asset in medicinal chemistry. Additionally, this compound's favorable solubility and stability characteristics enhance its usability in various formulations, ensuring consistent performance in laboratory and industrial applications.

Synonyms
2-Amino-4-methylthiophene-3-carboxylic acid ethyl ester
CAS Number
43088-42-2
Purity
≥ 98% (GC)
Molecular Formula
C8H11NO2S
Molecular Weight
185.24
MDL Number
MFCD00051669
PubChem ID
521132
Melting Point
79 - 83 °C
Appearance
Light yellow to yellow to orange crystalline powder
Conditions
Store at RT
General Information
Synonyms
2-Amino-4-methylthiophene-3-carboxylic acid ethyl ester
CAS Number
43088-42-2
Purity
≥ 98% (GC)
Molecular Formula
C8H11NO2S
Molecular Weight
185.24
MDL Number
MFCD00051669
PubChem ID
521132
Melting Point
79 - 83 °C
Appearance
Light yellow to yellow to orange crystalline powder
Conditions
Store at RT
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Ethyl 2-amino-4-methylthiophene-3-carboxylate is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as a building block in the synthesis of various pharmaceutical agents, particularly those targeting neurological disorders. Its unique structure can enhance bioavailability and efficacy.
  • Agricultural Chemistry: It is used in the formulation of agrochemicals, providing effective solutions for pest control. Its thiophene ring contributes to increased stability and effectiveness in various environmental conditions.
  • Material Science: The compound is explored in the development of novel materials, such as conductive polymers. Its properties can improve the performance of electronic devices, making them more efficient.
  • Biochemical Research: Researchers utilize this compound in studies related to enzyme inhibition and receptor binding, aiding in the understanding of biological pathways and potential therapeutic targets.
  • Cosmetic Formulations: It finds application in cosmetic products for its potential antioxidant properties, contributing to skin health and protection against environmental stressors.

Citations