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4-(3,4-dichlorophenyl)-3,4-dihydro-1(2H)-naphthalene-1-one 4-(3,4-dichloro-phenyl)-1-tetralone CAS:79560-19-3

4-(3,4-Dichlorophenyl)-3,4-dihydro-1(2H)-naphthalene-1-one, commonly referred to as 4-(3,4-dichlorophenyl)-1-tetralone, is an organic compound characterized by a fused ring system that includes a naphthalene unit and a carbonyl functionality. This compound is notable for its diverse pharmacological properties and has been studied for its potential applications in medicinal chemistry. The presence of the dichlorophenyl group enhances its biological activity and solubility, making it an interesting target for drug development. Ongoing research aims to explore its synthetic pathways and evaluate its efficacy in various therapeutic contexts.


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Application and Effect:

4-(3,4-Dichlorophenyl)-3,4-dihydro-1(2H)-naphthalene-1-one, or 4-(3,4-dichlorophenyl)-1-tetralone, is an intriguing compound due to its unique structure and potential biological activities. With the molecular formula C15H12Cl2O, this compound features a tetralone framework that includes a naphthalene moiety and a dichlorophenyl substituent. The structural arrangement leads to distinct chemical properties that make it suitable for various applications in medicinal chemistry and material science. One of the key areas of interest surrounding this compound is its potential pharmacological activity. Research has indicated that tetralones can exhibit a range of bioactivities, including anti-inflammatory, analgesic, and antimicrobial effects. The incorporation of the 3,4-dichlorophenyl group is particularly significant, as halogenated phenyl groups often enhance the interaction of molecules with biological targets, increasing their efficacy and selectivity. This characteristic encourages further investigation into its mechanism of action and therapeutic potential in treating conditions such as pain, inflammation, and infections. From a synthetic perspective, the preparation of 4-(3,4-dichlorophenyl)-1-tetralone can be achieved through various methods, including cyclization reactions involving precursors like substituted phenyl ketones or aldehydes. The ability to modify its structure through synthetic chemistry allows for the creation of derivatives with improved properties, which may lead to the discovery of new lead compounds in drug development. Furthermore, the compound's unique physical properties make it a candidate for use in materials science, where it could serve as a building block for polymers or functional materials. Its fluorescent properties might also be explored for applications in sensors or optoelectronic devices. In conclusion, 4-(3,4-dichlorophenyl)-3,4-dihydro-1(2H)-naphthalene-1-one stands out as a valuable compound in both medicinal chemistry and materials research. Its promising biological activities, along with its potential for structural modification, highlight the importance of continued research in unlocking its full therapeutic and industrial potential. As investigations progress, this compound may contribute significantly to advancements in drug discovery and application development.

Product Sample:

L-Arginine1
L-Arginine2

Product Packing:

L-Arginin3

Additional Information:

Composition C16H12Cl2O
Assay 99%
Appearance white powder
CAS No.  79560-19-3
Packing Small and bulk
Shelf Life 2 years
Storage Store in cool and dry area
Certification ISO.

 


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