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Catalog Number:
44288
CAS Number:
4815-32-1
Ethyl 2-amino-5-methylthiophene-3-carboxylate
Purity:
≥ 98% (GC)
Synonym(s):
2-Amino-5-methylthiophene-3-carboxylic acid ethyl ester
Documents
$184.18 /1G
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Product Information

Ethyl 2-amino-5-methylthiophene-3-carboxylate is a versatile compound with significant applications in the fields of pharmaceuticals and organic synthesis. This compound features a unique thiophene ring structure, which enhances its reactivity and makes it an excellent candidate for the development of novel therapeutic agents. Its amino and carboxylate functional groups allow for easy modification, enabling researchers to explore a variety of derivatives that can be tailored for specific biological activities.

In pharmaceutical research, Ethyl 2-amino-5-methylthiophene-3-carboxylate has been utilized in the synthesis of bioactive molecules, particularly in the development of anti-inflammatory and antimicrobial agents. Its ability to serve as a building block in complex organic reactions makes it invaluable for chemists looking to innovate in drug discovery. Additionally, its favorable solubility and stability characteristics enhance its utility in various formulations, providing a reliable option for researchers and industry professionals alike.

Synonyms
2-Amino-5-methylthiophene-3-carboxylic acid ethyl ester
CAS Number
4815-32-1
Purity
≥ 98% (GC)
Molecular Formula
C8H11NO2S
Molecular Weight
185.24
MDL Number
MFCD01922142
PubChem ID
4062885
Melting Point
47 - 51 °C
Appearance
White to almost white crystalline powder
Conditions
Store at RT
General Information
Synonyms
2-Amino-5-methylthiophene-3-carboxylic acid ethyl ester
CAS Number
4815-32-1
Purity
≥ 98% (GC)
Molecular Formula
C8H11NO2S
Molecular Weight
185.24
MDL Number
MFCD01922142
PubChem ID
4062885
Melting Point
47 - 51 °C
Appearance
White to almost white 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-5-methylthiophene-3-carboxylate is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as a building block in the synthesis of various pharmaceuticals, particularly in the development of drugs targeting neurological disorders due to its ability to interact with specific receptors in the brain.
  • Agricultural Chemistry: It is used in the formulation of agrochemicals, enhancing crop protection products. Its unique structure allows for improved efficacy against pests and diseases, leading to better yields.
  • Material Science: The compound is incorporated into the development of novel materials, such as conductive polymers, which are essential for applications in electronics and energy storage devices.
  • Biochemical Research: Researchers utilize this compound in studies involving enzyme inhibition, providing insights into metabolic pathways and potential therapeutic targets in various diseases.
  • Cosmetic Formulations: Its antioxidant properties make it a valuable ingredient in skincare products, helping to protect the skin from oxidative stress and improve overall skin health.

Citations