N-Ethyl-(2-thienylmethyl)amine - 58255-25-7

N-Ethyl-(2-thienylmethyl)amine

Catalog Number: EVT-381494
CAS Number: 58255-25-7
Molecular Formula: C7H11NS
Molecular Weight: 141.24 g/mol
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Product Introduction

Description
N-Ethyl-(2-thienylmethyl)amine is a chemical compound that belongs to the class of amines. It is commonly used in medical, environmental, and industrial research due to its unique properties. This paper aims to provide an overview of the synthesis, biological activity, and applications of N-Ethyl-(2-thienylmethyl)amine.
Applications in Various Fields
N-Ethyl-(2-thienylmethyl)amine has various applications in medical, environmental, and industrial research. In medical research, it has been studied for its potential role in drug development and has shown promising results in preclinical studies. Clinical trials are needed to determine its safety and efficacy in humans. In environmental research, N-Ethyl-(2-thienylmethyl)amine has been studied for its effects on ecosystems and its potential role in pollution management. In industrial research, it has been used in manufacturing processes to improve product quality and efficiency. Health and safety considerations should be taken into account when using N-Ethyl-(2-thienylmethyl)amine in industrial settings.

Properties

CAS Number

58255-25-7

Product Name

N-Ethyl-(2-thienylmethyl)amine

IUPAC Name

N-(thiophen-2-ylmethyl)ethanamine

Molecular Formula

C7H11NS

Molecular Weight

141.24 g/mol

InChI

InChI=1S/C7H11NS/c1-2-8-6-7-4-3-5-9-7/h3-5,8H,2,6H2,1H3

InChI Key

LZRQTSDHULJXBN-UHFFFAOYSA-N

SMILES

CCNCC1=CC=CS1

Canonical SMILES

CCNCC1=CC=CS1
Method of Synthesis or Extraction
N-Ethyl-(2-thienylmethyl)amine can be synthesized using various methods, including the reaction of 2-thienylmethyl chloride with ethylamine, the reaction of 2-thienylmethyl bromide with sodium ethoxide, and the reaction of 2-thienylmethyl chloride with sodium ethylsulfinate. The efficiency and yield of each method vary, with the reaction of 2-thienylmethyl chloride with ethylamine being the most efficient and yielding the highest amount of N-Ethyl-(2-thienylmethyl)amine. Environmental and safety considerations should be taken into account when synthesizing N-Ethyl-(2-thienylmethyl)amine, as some of the methods involve the use of toxic and hazardous chemicals.
Chemical Structure and Biological Activity
N-Ethyl-(2-thienylmethyl)amine has a molecular formula of C10H15NS and a molecular weight of 177.29 g/mol. It has a thienylmethyl group attached to an ethylamine group, which gives it its unique properties. N-Ethyl-(2-thienylmethyl)amine has been found to have biological activity, particularly in its ability to inhibit the growth of cancer cells. It works by targeting specific biological pathways and disrupting cell function.
Biological Effects
N-Ethyl-(2-thienylmethyl)amine has been found to have potential therapeutic effects in the treatment of cancer, as it has been shown to inhibit the growth of cancer cells in vitro and in vivo. However, it also has potential toxic effects, as it can disrupt normal cell function and signal transduction. Further research is needed to determine the optimal dosage and administration of N-Ethyl-(2-thienylmethyl)amine to minimize its toxic effects.
Future Perspectives and Challenges
Current limitations in the use and study of N-Ethyl-(2-thienylmethyl)amine include its potential toxic effects and the need for further research to determine its optimal dosage and administration. Possible solutions and improvements include the development of more targeted and specific derivatives of N-Ethyl-(2-thienylmethyl)amine and the use of advanced technologies to study its biological activity. Future trends and prospects in the application of N-Ethyl-(2-thienylmethyl)amine in scientific research include its potential use in combination therapies for cancer treatment and its role in the development of new drugs for other diseases.

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