Methyl 3-amino-4-methylthiophene-2-carboxylate - 85006-31-1

Methyl 3-amino-4-methylthiophene-2-carboxylate

Catalog Number: EVT-299928
CAS Number: 85006-31-1
Molecular Formula: C7H9NO2S
Molecular Weight: 171.22 g/mol
The product is for non-human research only. Not for therapeutic or veterinary use.
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Product Introduction

Description
Methyl 3-amino-4-methylthiophene-2-carboxylate is a heterocyclic compound that has gained significant attention in the scientific community due to its potential therapeutic and industrial applications. This paper aims to provide a comprehensive review of the synthesis, chemical structure, biological activity, effects, and applications of Methyl 3-amino-4-methylthiophene-2-carboxylate.
Applications in Various Fields
Methyl 3-amino-4-methylthiophene-2-carboxylate has potential applications in medical research, environmental research, and industrial research. In medical research, the compound may play a role in drug development and clinical trials for various diseases. In environmental research, Methyl 3-amino-4-methylthiophene-2-carboxylate may be used to study its effects on ecosystems and its role in pollution management. In industrial research, the compound may be used in manufacturing processes to improve product quality and efficiency. Health and safety considerations should be taken into account when using Methyl 3-amino-4-methylthiophene-2-carboxylate in these applications.

Properties

CAS Number

85006-31-1

Product Name

Methyl 3-amino-4-methylthiophene-2-carboxylate

IUPAC Name

methyl 3-amino-4-methylthiophene-2-carboxylate

Molecular Formula

C7H9NO2S

Molecular Weight

171.22 g/mol

InChI

InChI=1S/C7H9NO2S/c1-4-3-11-6(5(4)8)7(9)10-2/h3H,8H2,1-2H3

InChI Key

YICRPERKKBDRSP-UHFFFAOYSA-N

SMILES

CC1=CSC(=C1N)C(=O)OC

Synonyms

Methyl 3-Amino-4-Methylthiophene-2-Carboxylate

Canonical SMILES

CC1=CSC(=C1N)C(=O)OC
Method of Synthesis or Extraction
Methyl 3-amino-4-methylthiophene-2-carboxylate can be synthesized using various methods, including the Gewald reaction, the Hantzsch reaction, and the Pictet-Spengler reaction. The Gewald reaction involves the reaction of a ketone with a thiocarbamide and a cyanoacetamide in the presence of a base. The Hantzsch reaction involves the reaction of a β-ketoester, an aldehyde, and an ammonium salt in the presence of a reducing agent. The Pictet-Spengler reaction involves the reaction of an indole or a tryptamine with an aldehyde or a ketone in the presence of an acid. The efficiency and yield of each method vary depending on the starting materials, reaction conditions, and catalysts used. Environmental and safety considerations should also be taken into account when selecting a method for synthesis.
Chemical Structure and Biological Activity
Methyl 3-amino-4-methylthiophene-2-carboxylate has a heterocyclic structure consisting of a thiophene ring, an amino group, and a carboxylate group. The compound has been shown to exhibit various biological activities, including antimicrobial, antifungal, antitumor, and anti-inflammatory activities. The mechanism of action and biological targets of Methyl 3-amino-4-methylthiophene-2-carboxylate are not fully understood, but it is believed to interact with cellular enzymes and receptors.
Biological Effects
Methyl 3-amino-4-methylthiophene-2-carboxylate has been shown to affect cell function and signal transduction pathways. The compound has been found to inhibit the growth of cancer cells and reduce inflammation in animal models. However, the potential therapeutic and toxic effects of Methyl 3-amino-4-methylthiophene-2-carboxylate in humans are not well established and require further investigation.
Future Perspectives and Challenges
The use and study of Methyl 3-amino-4-methylthiophene-2-carboxylate face several limitations, including its low solubility and stability. Possible solutions and improvements include the development of new synthesis methods and the modification of the compound's chemical structure. Future trends and prospects in the application of Methyl 3-amino-4-methylthiophene-2-carboxylate in scientific research include its potential use in personalized medicine and the development of new therapeutic agents. However, further research is needed to fully understand the compound's biological activity and potential applications.
In conclusion, Methyl 3-amino-4-methylthiophene-2-carboxylate is a promising compound with potential applications in various fields. Its synthesis, chemical structure, biological activity, effects, and applications have been reviewed in this paper. Further research is needed to fully understand the compound's potential and limitations.

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