4-Chlorothiophene-2-carbaldehyde - 57500-51-3

4-Chlorothiophene-2-carbaldehyde

Catalog Number: EVT-343127
CAS Number: 57500-51-3
Molecular Formula: C5H3ClOS
Molecular Weight: 146.6 g/mol
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Product Introduction

Description
4-Chlorothiophene-2-carbaldehyde is a heterocyclic organic compound that belongs to the family of thiophene derivatives. It is widely used in various fields, including medical, environmental, and industrial research. This paper aims to provide a comprehensive review of the synthesis, chemical structure, biological activity, biological effects, applications, future perspectives, and challenges of 4-Chlorothiophene-2-carbaldehyde.
Applications in Various Fields
In medical research, 4-Chlorothiophene-2-carbaldehyde has been used in drug development, particularly in the development of anticancer and antimicrobial agents. It has also been used in clinical trials, where it has shown promising results in the treatment of various diseases. However, its potential side effects and toxicity should be carefully considered before using it in clinical settings. In environmental research, 4-Chlorothiophene-2-carbaldehyde has been found to have effects on ecosystems and can be used in pollution management. In industrial research, it has been used in manufacturing processes to improve product quality and efficiency, but health and safety considerations should be taken into account.

Properties

CAS Number

57500-51-3

Product Name

4-Chlorothiophene-2-carbaldehyde

IUPAC Name

4-chlorothiophene-2-carbaldehyde

Molecular Formula

C5H3ClOS

Molecular Weight

146.6 g/mol

InChI

InChI=1S/C5H3ClOS/c6-4-1-5(2-7)8-3-4/h1-3H

InChI Key

YYEIZVYJDLYMIH-UHFFFAOYSA-N

SMILES

C1=C(SC=C1Cl)C=O

Canonical SMILES

C1=C(SC=C1Cl)C=O
Method of Synthesis or Extraction
There are several methods for synthesizing 4-Chlorothiophene-2-carbaldehyde, including the Vilsmeier-Haack reaction, the Gewald reaction, and the Pinner reaction. The Vilsmeier-Haack reaction is the most commonly used method, which involves the reaction of 4-chlorothiophene with DMF and POCl3. The Gewald reaction involves the reaction of 2-cyanothioacetamide with a halogenated aldehyde, while the Pinner reaction involves the reaction of 4-chlorothiophene with an alkyl nitrite and hydrochloric acid. The efficiency and yield of each method vary, with the Vilsmeier-Haack reaction being the most efficient and yielding the highest amount of 4-Chlorothiophene-2-carbaldehyde. Environmental and safety considerations should be taken into account when using these methods, as they involve the use of toxic and hazardous chemicals.
Chemical Structure and Biological Activity
The chemical structure of 4-Chlorothiophene-2-carbaldehyde consists of a thiophene ring with a chloro substituent and an aldehyde group. It has been found to exhibit various biological activities, including antimicrobial, antifungal, and anticancer activities. The mechanism of action and biological targets of 4-Chlorothiophene-2-carbaldehyde are not fully understood, but it is believed to act by inhibiting the growth and proliferation of cancer cells and microorganisms.
Biological Effects
4-Chlorothiophene-2-carbaldehyde has been shown to have potential therapeutic effects on cell function and signal transduction. It has been found to inhibit the growth of cancer cells and microorganisms, and to induce apoptosis in cancer cells. However, it also has potential toxic effects, as it can cause DNA damage and oxidative stress. Further studies are needed to determine the optimal dosage and duration of treatment to minimize the toxic effects of 4-Chlorothiophene-2-carbaldehyde.
Future Perspectives and Challenges
The use and study of 4-Chlorothiophene-2-carbaldehyde are currently limited by its potential toxicity and side effects. Possible solutions and improvements include the development of more efficient and safer synthesis methods, the identification of its mechanism of action and biological targets, and the optimization of its dosage and duration of treatment. Future trends and prospects in the application of 4-Chlorothiophene-2-carbaldehyde in scientific research include its potential use in the development of novel drugs and therapies, as well as its potential use in environmental and industrial research.
Conclusion:
In conclusion, 4-Chlorothiophene-2-carbaldehyde is a heterocyclic organic compound that has various applications in medical, environmental, and industrial 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 mechanism of action and biological targets, as well as to optimize its use in various fields.

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