Ethyl thiophene-3-carboxylate - 5751-80-4

Ethyl thiophene-3-carboxylate

Catalog Number: EVT-301328
CAS Number: 5751-80-4
Molecular Formula: C7H8O2S
Molecular Weight: 156.2 g/mol
The product is for non-human research only. Not for therapeutic or veterinary use.
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Product Introduction

Description
Ethyl thiophene-3-carboxylate is a chemical compound that belongs to the class of thiophene carboxylates. It is a colorless to pale yellow liquid with a fruity odor. Ethyl thiophene-3-carboxylate has gained significant attention in scientific research due to its potential biological and industrial applications.
Applications in Various Fields
Ethyl thiophene-3-carboxylate has potential applications in medical, environmental, and industrial research. In medical research, it may have a role in drug development, clinical trials, and findings. It may also have benefits and potential side effects in the treatment of inflammatory diseases and cancer. In environmental research, it may have effects on ecosystems, a role in pollution management, and sustainability and environmental impact. In industrial research, it may have a use in manufacturing processes, improving product quality and efficiency, and health and safety considerations.

Properties

CAS Number

5751-80-4

Product Name

Ethyl thiophene-3-carboxylate

IUPAC Name

ethyl thiophene-3-carboxylate

Molecular Formula

C7H8O2S

Molecular Weight

156.2 g/mol

InChI

InChI=1S/C7H8O2S/c1-2-9-7(8)6-3-4-10-5-6/h3-5H,2H2,1H3

InChI Key

OYSLMAQEMAJMCL-UHFFFAOYSA-N

SMILES

CCOC(=O)C1=CSC=C1

Canonical SMILES

CCOC(=O)C1=CSC=C1
Method of Synthesis or Extraction
Ethyl thiophene-3-carboxylate can be synthesized by various methods, including the reaction of thiophene-3-carboxylic acid with ethanol in the presence of a catalyst, the reaction of thiophene-3-carboxylic acid with ethyl chloroformate, and the reaction of thiophene-3-carboxylic acid with ethyl diazoacetate. The efficiency and yield of each method vary depending on the reaction conditions and the purity of the starting materials. The environmental and safety considerations of these methods include the use of hazardous chemicals, the generation of waste, and the potential for explosion and fire.
Chemical Structure and Biological Activity
The chemical structure of ethyl thiophene-3-carboxylate consists of a thiophene ring attached to a carboxylate group and an ethyl group. The mechanism of action and biological targets of ethyl thiophene-3-carboxylate are not fully understood. However, studies have shown that it exhibits potent anti-inflammatory, antioxidant, and anticancer activities. The bioactivity and potency of ethyl thiophene-3-carboxylate depend on the concentration, duration of exposure, and the type of cells or organisms used in the experiments.
Biological Effects
Ethyl thiophene-3-carboxylate has been shown to affect cell function and signal transduction pathways. It can induce apoptosis, inhibit cell proliferation, and modulate the expression of genes involved in inflammation and cancer. The potential therapeutic and toxic effects of ethyl thiophene-3-carboxylate are still under investigation. However, it has been suggested that it may have a role in the treatment of inflammatory diseases, such as rheumatoid arthritis, and cancer.
Future Perspectives and Challenges
The current limitations in the use and study of ethyl thiophene-3-carboxylate include the lack of understanding of its mechanism of action and biological targets, the need for more extensive studies on its toxicity and safety, and the challenges in scaling up the synthesis process. Possible solutions and improvements include the development of new synthetic methods, the use of advanced analytical techniques to study its biological activity, and the optimization of its formulation for therapeutic applications. Future trends and prospects in the application of ethyl thiophene-3-carboxylate in scientific research include the exploration of its potential as a drug candidate, the investigation of its role in environmental sustainability, and the development of new industrial applications.
In conclusion, ethyl thiophene-3-carboxylate is a promising chemical compound with potential applications in various fields of research. Its synthesis, chemical structure, biological activity, biological effects, applications, future perspectives, and challenges have been discussed in this paper. Further studies are needed to fully understand its potential and limitations in scientific research.

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