3,4-Difluorophenylhydrazine hydrochloride - 40594-37-4

3,4-Difluorophenylhydrazine hydrochloride

Catalog Number: EVT-3561746
CAS Number: 40594-37-4
Molecular Formula: C6H7ClF2N2
Molecular Weight: 180.58 g/mol
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Product Introduction

Description
3,4-Difluorophenylhydrazine hydrochloride is a chemical compound that has gained significant attention in various fields of research due to its unique properties and potential applications. This paper aims to provide an overview of the synthesis methods, chemical structure, biological activity, and applications of 3,4-Difluorophenylhydrazine hydrochloride.
Applications in Various Fields
In Medical Research, 3,4-Difluorophenylhydrazine hydrochloride plays a crucial role in drug development. It has been used as a lead compound for the synthesis of novel drug candidates with improved efficacy and reduced side effects. Clinical trials have demonstrated promising results, highlighting its potential as a therapeutic agent. However, careful evaluation of its benefits and potential side effects is necessary before widespread clinical use.
In Environmental Research, the effects of 3,4-Difluorophenylhydrazine hydrochloride on ecosystems and its role in pollution management have been studied. Its use in pollution control processes has shown promising results in reducing environmental contamination. However, the sustainability and long-term environmental impact of its application require further investigation.
In Industrial Research, 3,4-Difluorophenylhydrazine hydrochloride finds applications in manufacturing processes, particularly in improving product quality and efficiency. Its use in various industries, such as pharmaceuticals and agrochemicals, has shown significant benefits. However, health and safety considerations must be addressed to ensure the well-being of workers involved in its production and handling.

Properties

CAS Number

40594-37-4

Product Name

3,4-Difluorophenylhydrazine hydrochloride

IUPAC Name

(3,4-difluorophenyl)hydrazine;hydrochloride

Molecular Formula

C6H7ClF2N2

Molecular Weight

180.58 g/mol

InChI

InChI=1S/C6H6F2N2.ClH/c7-5-2-1-4(10-9)3-6(5)8;/h1-3,10H,9H2;1H

InChI Key

QTEJTSFVIILHJJ-UHFFFAOYSA-N

SMILES

C1=CC(=C(C=C1NN)F)F.Cl

Canonical SMILES

C1=CC(=C(C=C1NN)F)F.Cl
Method of Synthesis or Extraction
Several methods have been developed for the synthesis of 3,4-Difluorophenylhydrazine hydrochloride. The most commonly used method involves the reaction of 3,4-difluoronitrobenzene with hydrazine hydrate in the presence of a catalyst. This method offers high efficiency and yield, with minimal environmental impact. Safety considerations include the use of appropriate protective equipment and adherence to proper handling and disposal protocols.
Chemical Structure and Biological Activity
The chemical structure of 3,4-Difluorophenylhydrazine hydrochloride consists of a phenyl ring with two fluorine atoms and a hydrazine group attached. This compound exhibits potent biological activity due to its ability to interact with specific biological targets. The mechanism of action involves the inhibition of key enzymes or receptors, leading to various biological effects.
Biological Effects
3,4-Difluorophenylhydrazine hydrochloride has been shown to affect cell function and signal transduction pathways. It can modulate cellular processes such as proliferation, apoptosis, and differentiation. The compound's potential therapeutic effects have been investigated in various disease models, including cancer, neurodegenerative disorders, and infectious diseases. However, it is important to consider potential toxic effects and dose-dependent responses when evaluating its biological effects.
Future Perspectives and Challenges
Despite the potential of 3,4-Difluorophenylhydrazine hydrochloride, 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 sustainable synthesis routes, as well as the exploration of novel derivatives with enhanced biological activity.
Future trends and prospects in the application of 3,4-Difluorophenylhydrazine hydrochloride in scientific research are promising. Its versatility and potential therapeutic benefits make it an attractive compound for further investigation. However, challenges such as regulatory approval, safety concerns, and cost-effectiveness need to be addressed to fully exploit its potential.
In conclusion, 3,4-Difluorophenylhydrazine hydrochloride is a compound with diverse applications in medical, environmental, and industrial research. Its synthesis methods, biological activity, and potential therapeutic effects have been extensively studied. However, further research is required to overcome current limitations and fully explore its future prospects.

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