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Catalog Number:
24158
CAS Number:
76575-71-8
Methyl 3-amino-5-methylthiophene-2-carboxylate
Purity:
≥ 97% (GC)
Synonym(s):
3-Amino-5-methyl-thiophene-2-carboxylic acid methyl ester
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Product Information

Methyl 3-amino-5-methylthiophene-2-carboxylate is a versatile compound widely utilized in the synthesis of various pharmaceuticals and agrochemicals. This compound features a unique thiophene ring structure, which enhances its reactivity and makes it an essential building block in the development of biologically active molecules. Its amino and carboxylate functional groups contribute to its solubility and compatibility with a range of chemical reactions, making it suitable for applications in medicinal chemistry and organic synthesis.

Researchers and industry professionals appreciate Methyl 3-amino-5-methylthiophene-2-carboxylate for its role in the creation of novel therapeutic agents, particularly in the fields of anti-inflammatory and antimicrobial drug development. Its distinct properties allow for the fine-tuning of molecular interactions, leading to improved efficacy and reduced side effects in drug formulations. Additionally, this compound can serve as a precursor in the synthesis of agrochemicals, enhancing crop protection and yield. With its broad applicability and significant advantages over similar compounds, Methyl 3-amino-5-methylthiophene-2-carboxylate is an invaluable asset for innovative research and development.

Synonyms
3-Amino-5-methyl-thiophene-2-carboxylic acid methyl ester
CAS Number
76575-71-8
Purity
≥ 97% (GC)
Molecular Formula
C7H9NO2S
Molecular Weight
171.22
MDL Number
MFCD00130095
PubChem ID
818952
Appearance
Yellow solid
Conditions
Store at 0-8 °C
General Information
Synonyms
3-Amino-5-methyl-thiophene-2-carboxylic acid methyl ester
CAS Number
76575-71-8
Purity
≥ 97% (GC)
Molecular Formula
C7H9NO2S
Molecular Weight
171.22
MDL Number
MFCD00130095
PubChem ID
818952
Appearance
Yellow solid
Conditions
Store at 0-8 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Methyl 3-amino-5-methylthiophene-2-carboxylate is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as a key intermediate in synthesizing various pharmaceuticals, particularly those targeting neurological disorders, due to its ability to interact with specific receptors in the brain.
  • Agricultural Chemicals: It is used in the formulation of agrochemicals, enhancing the efficacy of pesticides and herbicides by improving their absorption and effectiveness on target plants.
  • Organic Synthesis: This chemical is a valuable building block in organic synthesis, allowing researchers to create complex molecules for materials science and nanotechnology applications.
  • Colorants and Dyes: Its unique structure makes it suitable for developing vibrant colorants and dyes used in textiles and coatings, providing excellent stability and colorfastness.
  • Research in Biochemistry: The compound is employed in biochemical studies to explore enzyme interactions and metabolic pathways, contributing to advancements in understanding cellular processes.

Citations