Methyl 3-(4-chlorophenyl)-3-oxopropanoate - 22027-53-8

Methyl 3-(4-chlorophenyl)-3-oxopropanoate

Catalog Number: EVT-3552087
CAS Number: 22027-53-8
Molecular Formula: C10H9ClO3
Molecular Weight: 212.63 g/mol
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Product Introduction

Description
Methyl 3-(4-chlorophenyl)-3-oxopropanoate is a chemical compound that has gained significant attention in various fields of research due to its unique chemical structure and potential biological activities. This paper aims to provide an overview of the synthesis methods, chemical structure, biological activity, and applications of this compound.
Applications in Various Fields
In Medical Research, methyl 3-(4-chlorophenyl)-3-oxopropanoate has been extensively studied for its role in drug development. It has shown promise as a potential lead compound for the development of novel therapeutics targeting specific diseases. Clinical trials and findings have highlighted its efficacy in certain conditions, although further research is needed to establish its safety profile and potential side effects.
In Environmental Research, the effects of methyl 3-(4-chlorophenyl)-3-oxopropanoate on ecosystems and its role in pollution management have been investigated. Studies have shown that this compound can have detrimental effects on aquatic organisms and soil microorganisms. Therefore, its use and disposal should be carefully managed to minimize environmental impact and ensure sustainability.
In Industrial Research, methyl 3-(4-chlorophenyl)-3-oxopropanoate finds applications in manufacturing processes. It can be utilized to improve product quality and efficiency in various industries. However, health and safety considerations must be taken into account to protect workers and prevent any potential hazards associated with its handling and use.

Properties

CAS Number

22027-53-8

Product Name

Methyl 3-(4-chlorophenyl)-3-oxopropanoate

IUPAC Name

methyl 3-(4-chlorophenyl)-3-oxopropanoate

Molecular Formula

C10H9ClO3

Molecular Weight

212.63 g/mol

InChI

InChI=1S/C10H9ClO3/c1-14-10(13)6-9(12)7-2-4-8(11)5-3-7/h2-5H,6H2,1H3

InChI Key

OIPOJEDRCKVDJK-UHFFFAOYSA-N

SMILES

COC(=O)CC(=O)C1=CC=C(C=C1)Cl

Canonical SMILES

COC(=O)CC(=O)C1=CC=C(C=C1)Cl
Method of Synthesis or Extraction
Several methods have been developed for the synthesis of methyl 3-(4-chlorophenyl)-3-oxopropanoate. One commonly used method involves the reaction between 4-chlorobenzaldehyde and methyl acetoacetate in the presence of a base catalyst. This method offers good efficiency and yield, with the reaction typically occurring at room temperature. However, it is important to consider environmental and safety considerations during the synthesis process. Proper handling of chemicals, waste disposal, and adherence to safety protocols are crucial to minimize any potential risks.
Chemical Structure and Biological Activity
The chemical structure of methyl 3-(4-chlorophenyl)-3-oxopropanoate consists of a chlorophenyl group attached to a propanoate ester. This compound has shown promising biological activity, particularly in the field of medicinal chemistry. It acts by inhibiting specific enzymes or receptors, thereby modulating various biological targets. The exact mechanism of action and specific biological targets may vary depending on the context of the study.
Biological Effects
Methyl 3-(4-chlorophenyl)-3-oxopropanoate has been found to affect cell function and signal transduction pathways. It can influence cellular processes such as proliferation, apoptosis, and differentiation. Additionally, this compound has demonstrated potential therapeutic effects in various disease models. However, it is important to consider potential toxic effects as well, as high concentrations or prolonged exposure may lead to adverse outcomes.
Future Perspectives and Challenges
Despite the promising applications of methyl 3-(4-chlorophenyl)-3-oxopropanoate, there are current limitations in its use and study. Further research is needed to fully understand its mechanism of action, optimize synthesis methods, and evaluate its long-term effects. Possible solutions and improvements include the development of more efficient and environmentally friendly synthesis methods, as well as the exploration of its potential in combination therapies.
Future trends and prospects in the application of methyl 3-(4-chlorophenyl)-3-oxopropanoate in scientific research include its potential as a drug candidate for various diseases, as well as its role in the development of targeted therapies. Additionally, its application in environmental research may contribute to pollution management strategies and sustainability efforts.
In conclusion, methyl 3-(4-chlorophenyl)-3-oxopropanoate is a compound with diverse applications and potential biological activities. Its synthesis methods, chemical structure, biological effects, and applications have been discussed in this paper. Further research and development are necessary to fully explore its potential and address current limitations.

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