4-Chloro-2-methoxybenzyl alcohol - 55685-75-1

4-Chloro-2-methoxybenzyl alcohol

Catalog Number: EVT-3563473
CAS Number: 55685-75-1
Molecular Formula: C8H9ClO2
Molecular Weight: 172.61 g/mol
The product is for non-human research only. Not for therapeutic or veterinary use.
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Product Introduction

Description
4-Chloro-2-methoxybenzyl alcohol is a chemical compound that belongs to the class of benzyl alcohols. It is widely used in various fields, including medical, environmental, and industrial research. This paper aims to provide a comprehensive overview of the synthesis methods, chemical structure, biological activity, effects on cell function and signal transduction, applications in different research areas, and future perspectives and challenges associated with 4-Chloro-2-methoxybenzyl alcohol.
Applications in Various Fields
In medical research, 4-Chloro-2-methoxybenzyl alcohol plays a crucial role in drug development. It has been used as a starting material for the synthesis of novel compounds with potential therapeutic properties. Clinical trials have shown promising results in the treatment of certain diseases, although further research is needed to fully understand its benefits and potential side effects. In environmental research, this compound has been studied for its effects on ecosystems and its role in pollution management. It has shown potential in the removal of pollutants from water and soil, contributing to sustainability and minimizing environmental impact. In industrial research, 4-Chloro-2-methoxybenzyl alcohol is used in manufacturing processes to improve product quality and efficiency. However, health and safety considerations must be taken into account to ensure the well-being of workers and minimize potential risks.

Properties

CAS Number

55685-75-1

Product Name

4-Chloro-2-methoxybenzyl alcohol

IUPAC Name

(4-chloro-2-methoxyphenyl)methanol

Molecular Formula

C8H9ClO2

Molecular Weight

172.61 g/mol

InChI

InChI=1S/C8H9ClO2/c1-11-8-4-7(9)3-2-6(8)5-10/h2-4,10H,5H2,1H3

InChI Key

AXXPZAITCCIOIA-UHFFFAOYSA-N

SMILES

COC1=C(C=CC(=C1)Cl)CO

Canonical SMILES

COC1=C(C=CC(=C1)Cl)CO
Method of Synthesis or Extraction
Several methods are commonly used for the synthesis of 4-Chloro-2-methoxybenzyl alcohol. One of the most efficient methods involves the reaction of 4-chloro-2-methoxybenzaldehyde with sodium borohydride in the presence of a suitable solvent. This method offers a high yield of the desired product and is relatively safe and environmentally friendly. Another method involves the reduction of 4-chloro-2-methoxybenzaldehyde using a reducing agent such as lithium aluminum hydride. However, this method may have lower yields and pose higher safety risks.
Chemical Structure and Biological Activity
The chemical structure of 4-Chloro-2-methoxybenzyl alcohol consists of a benzene ring with a chlorine atom and a methoxy group attached to a carbon atom, which is further connected to an alcohol functional group. This compound exhibits various biological activities and has been found to interact with specific biological targets. The mechanism of action involves the modulation of signal transduction pathways, leading to specific biological effects.
Biological Effects
The biological effects of 4-Chloro-2-methoxybenzyl alcohol on cell function and signal transduction are diverse. It has been shown to affect cell proliferation, apoptosis, and differentiation processes. Additionally, it can modulate various signaling pathways, including MAPK, PI3K/Akt, and NF-κB, which are involved in cell survival, inflammation, and immune responses. These effects make 4-Chloro-2-methoxybenzyl alcohol a potential therapeutic agent, but also raise concerns about potential toxic effects.
Future Perspectives and Challenges
Despite the potential applications of 4-Chloro-2-methoxybenzyl alcohol, there are current limitations in its use and study. The compound's stability, solubility, and bioavailability need to be further optimized to enhance its efficacy and reduce potential side effects. Additionally, more research is required to fully understand its mechanism of action and identify its specific biological targets. Future trends and prospects in the application of 4-Chloro-2-methoxybenzyl alcohol in scientific research include the development of more potent derivatives and the exploration of its potential in combination therapies. Overcoming these challenges will pave the way for the successful utilization of 4-Chloro-2-methoxybenzyl alcohol in various research fields.
In conclusion, 4-Chloro-2-methoxybenzyl alcohol is a versatile compound with significant potential in medical, environmental, and industrial research. Its synthesis methods, chemical structure, biological activity, effects on cell function and signal transduction, applications, and future perspectives have been discussed in this paper. Further research and development are needed to fully exploit the benefits of this compound while addressing the associated challenges.

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