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4-[[(4-Fluorophenyl)imino]methyl]-phenol CAS:3382-63-6

4-[[(4-Fluorophenyl)imino]methyl]-phenol is a chemical compound distinguished by its molecular structure, featuring a phenolic ring attached to a 4-fluorophenyl imine group. This configuration imbues the compound with unique chemical properties that are significant in both pharmaceutical and industrial applications. Synthesized through specialized organic chemistry techniques, this compound serves as a versatile building block in the development of pharmaceuticals and functional materials, owing to its distinctive structural motifs and reactivity.


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4-[[(4-Fluorophenyl)imino]methyl]-phenol is characterized by its intricate molecular structure and diverse applications, explored comprehensively below. Chemical Structure and Properties The compound's structure consists of a phenolic ring linked to a 4-fluorophenyl imine group, where the imine carbon is attached directly to the phenolic oxygen. This arrangement influences its chemical behavior, affecting solubility, stability, and interactions with other molecules or surfaces. The presence of the fluorophenyl imine moiety introduces specific electronic and steric effects that are crucial for its biological and industrial applications. Synthesis Methods and Applications Synthesis of 4-[[(4-Fluorophenyl)imino]methyl]-phenol typically involves the condensation reaction between a phenol derivative and a fluorophenyl amine under controlled conditions. The process requires precise control over reaction parameters to achieve high purity and yield, ensuring the compound's suitability for various applications. Its synthesis pathway underscores its potential as a versatile intermediate in pharmaceutical and material science research. Pharmacological and Industrial Relevance In pharmacology, this compound exhibits potential bioactive properties due to its structural resemblance to pharmacologically active molecules. Research focuses on its role as a precursor in the synthesis of therapeutic agents targeting specific biological pathways or disease mechanisms. Moreover, in industrial applications, 4-[[(4-Fluorophenyl)imino]methyl]-phenol contributes to the development of functional materials such as coatings or adhesives, where its chemical reactivity and structural attributes enhance performance characteristics. Environmental and Technological Applications Beyond its pharmaceutical and industrial uses, this compound holds promise in environmental applications, including the synthesis of environmentally friendly materials or catalysts. Its chemical versatility allows for modifications that can tailor its properties to meet specific requirements in sustainability and industrial efficiency. Conclusion 4-[[(4-Fluorophenyl)imino]methyl]-phenol stands out as a significant compound in both pharmaceutical and industrial contexts, driven by its unique structural composition and reactivity. Its synthesis and application in diverse fields underscore ongoing efforts to innovate in drug discovery, material science, and environmental technology. Future research endeavors will likely focus on optimizing synthesis methodologies, exploring novel applications, and uncovering new potential benefits of this compound in addressing current scientific and industrial challenges.

4-[[(4-Fluorophenyl)imino]methyl]-phenol is characterized by its intricate molecular structure and diverse applications, explored comprehensively below. Chemical Structure and Properties The compound's structure consists of a phenolic ring linked to a 4-fluorophenyl imine group, where the imine carbon is attached directly to the phenolic oxygen. This arrangement influences its chemical behavior, affecting solubility, stability, and interactions with other molecules or surfaces. The presence of the fluorophenyl imine moiety introduces specific electronic and steric effects that are crucial for its biological and industrial applications. Synthesis Methods and Applications Synthesis of 4-[[(4-Fluorophenyl)imino]methyl]-phenol typically involves the condensation reaction between a phenol derivative and a fluorophenyl amine under controlled conditions. The process requires precise control over reaction parameters to achieve high purity and yield, ensuring the compound's suitability for various applications. Its synthesis pathway underscores its potential as a versatile intermediate in pharmaceutical and material science research. Pharmacological and Industrial Relevance In pharmacology, this compound exhibits potential bioactive properties due to its structural resemblance to pharmacologically active molecules. Research focuses on its role as a precursor in the synthesis of therapeutic agents targeting specific biological pathways or disease mechanisms. Moreover, in industrial applications, 4-[[(4-Fluorophenyl)imino]methyl]-phenol contributes to the development of functional materials such as coatings or adhesives, where its chemical reactivity and structural attributes enhance performance characteristics. Environmental and Technological Applications Beyond its pharmaceutical and industrial uses, this compound holds promise in environmental applications, including the synthesis of environmentally friendly materials or catalysts. Its chemical versatility allows for modifications that can tailor its properties to meet specific requirements in sustainability and industrial efficiency. Conclusion 4-[[(4-Fluorophenyl)imino]methyl]-phenol stands out as a significant compound in both pharmaceutical and industrial contexts, driven by its unique structural composition and reactivity. Its synthesis and application in diverse fields underscore ongoing efforts to innovate in drug discovery, material science, and environmental technology. Future research endeavors will likely focus on optimizing synthesis methodologies, exploring novel applications, and uncovering new potential benefits of this compound in addressing current scientific and industrial challenges.

Product Sample:

L-Arginine1
L-Arginine2

Product Packing:

L-Arginin3

Additional Information:

Composition C13H10FNO
Assay 99%
Appearance white powder
CAS No.  3382-63-6
Packing Small and bulk
Shelf Life 2 years
Storage Store in cool and dry area
Certification ISO.

 


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