6280-53-1

Usage

Uses

Used in Pharmaceutical Synthesis:
(2-chlorophenyl)(4-hydroxy-3-methylphenyl)methanone is used as an intermediate in the synthesis of pharmaceuticals due to its unique structure and functional groups. Its presence in the molecular framework can contribute to the development of new drugs with specific therapeutic properties.
Used in Agrochemical Production:
(2-chlorophenyl)(4-hydroxy-3-methylphenyl)methanone is also utilized as an intermediate in the production of agrochemicals, where it can be incorporated into the design of new pesticides or other agricultural products to enhance their effectiveness and selectivity.
Used in Organic Synthesis:
(2-chlorophenyl)(4-hydroxy-3-methylphenyl)methanone serves as a building block in organic synthesis, allowing for the creation of a variety of complex organic molecules. Its versatility in forming different chemical bonds and its stability make it a valuable component in the synthesis of specialty chemicals.
(Note: The specific applications and properties of (2-chlorophenyl)(4-hydroxy-3-methylphenyl)methanone would need to be confirmed through further research and testing, as the provided materials do not detail the exact uses or reasons for its application in various industries.)

Upstream product

• 6279-32-9 2-methylphenyl 2-chlorobenzoate 
• 95-48-7 ortho-cresol 
• 609-65-4 o-chlorobenzoyl chloride 

Downstream Products

• 110029-32-8 4-(2-chloro-benzyl)-2-methyl-phenol 
• 114330-13-1 4-(2-chloro-benzyl)-1-(3,5-dinitro-benzoyloxy)-2-methyl-benzene 

Relevant academic research and scientific papers

TETRAZOLINONE COMPOUND AND APPLICATIONS THEREOF

Disclosed is a tetrazolinone compound having a high pest control effect and represented by the formula (1): wherein R1, R2, R3, and R11 each represent a halogen atom, a C1-C6 alkyl group, or the like; R4 and R5 each represent a hydrogen atom, a halogen atom, a C1-C3 alkyl group, or the like; R6 represents a C1-C3 alkyl group which may have a halogen atom(s) or the like; R7, R8, and R9 each represent a hydrogen atom, a halogen atom, or the like; R10 represents a C1-C3 alkyl group or the like; R12 represents a C1-C6 alkyl group, a C3-C6 cycloalkyl group, or the like, and R13 represents a C1-C6 alkyl group, a C2-C6 alkenyl group, or the like.

Synthesis, xanthine oxidase inhibition, and antioxidant screening of benzophenone tagged thiazolidinone analogs

A series of novel 2-(diaryl methanone)-N-(4-oxo-2-phenyl-thiazolidin-3-yl)- acetamides were synthesized by various Schiff bases of (4-benzoyl-phenoxy)-aceto hydrazide with thioglycolic acid. The structures of the newly synthesized compounds were confirmed

Design, synthesis, and anticancer properties of novel benzophenone- conjugated coumarin analogs

In the current scenario, development of anticancer drugs with specific targets is of prime importance in modern chemical biology. Observing the importance of benzophenone and coumarin nucleus, it would be worthwhile to design and synthesize novel benzophenone derivatives (8a-o) bearing the coumarin nucleus. Further, they were screened for prospective anticancer activities in vitro against the Michigan Cancer Foundation-7 (MCF-7) and Ehrlich's ascites tumor (EAT) cell lines and their biomarkers, followed by in silico studies regarding phosphoinositide 3-kinase (PI3K) and caspase by molecular docking. Benzophenones have been reported as potential drugs targeting tumor angiogenesis; thus, the formation of neovessels in an in vivo model system like CAM, which is angiogenesis dependent, was observed in the presence of compounds 8a-o. The above findings would help in understanding their putative potential as therapeutic agents for cancer patients. Coumarin-integrated benzophenone conjugates (8a-o) were designed, synthesized, and screened for prospective anticancer activities in vitro against the MCF-7 and EAT cell lines. Molecular docking studies with regard to phosphoinositide 3-kinase and caspase were performed. In addition, neovessel formation was observed in an in vivo model system.