10325-65-2

Usage

Uses

Used in Pharmaceutical Industry:
2,3-dibromo-1-(4-methylphenyl)-3-phenylpropan-1-one is used as a building block for the preparation of various pharmaceuticals. Its unique reactivity and structural features make it a promising candidate for the development of new drugs in the field of medicinal chemistry.
Used in Agrochemical Industry:
In the agrochemical industry, 2,3-dibromo-1-(4-methylphenyl)-3-phenylpropan-1-one serves as a key intermediate in the synthesis of various agrochemicals. Its reactivity and versatility in chemical reactions contribute to the development of effective and targeted agrochemical products.
Used in Organic Synthesis:
2,3-dibromo-1-(4-methylphenyl)-3-phenylpropan-1-one is utilized as a reactant in the formation of other complex organic molecules. Its presence in organic synthesis allows for the creation of a wide range of compounds with diverse applications across various industries.

Upstream product

• 4224-96-8 3-phenyl-1-p-tolylprop-2-en-1-one 
• 50603-93-5 α-bromo-4'-methyl-chalcone 
• 14802-30-3 (E)-1-(4-methylphenyl)-3-phenyl-2-propen-1-one 
• 30925-52-1 (2Z)-3-(4-methoxyphenyl)-1-phenylprop-2-en-1-one 
• 122-00-9 para-methylacetophenone 
• 100-52-7 benzaldehyde 

Downstream Products

• 6372-29-8 cis-1-cyclohexyl-2-phenyl-3-(p-toluyl)aziridine 
• 6372-29-8 trans-1-cyclohexyl-2-phenyl-3-(p-toluyl)aziridine 
• 1427302-08-6 (Z)-2-azido-3-phenyl-1-(p-tolyl)prop-2-en-1-one 
• 100321-77-5 (4,5-diphenyl-1H-pyrazol-3-yl)(p-tolyl)methanone 
• 32045-93-5 2,3-dimorpholino-3-phenyl-1-(p-tolyl)propan-1-one 
• 25855-99-6 1-(4-methylphenyl)-3-phenyl-1,3-propanedione 
• 50603-93-5 (Z)-2-Bromo-3-phenyl-1-p-tolyl-propenone 
• 54458-30-9 2-bromo-1-(4-methylphenyl)-3-phenyl-1,3-propanedione 
• 54458-33-2 1-phenyl-3-(p-tolyl)propane-1,2,3-trione 

Relevant academic research and scientific papers

Modular access to 1,2-allenyl ketones based on a photoredox-catalysed radical-polar crossover process

Herein, a new protocol dealing with the preparation of 1,2-allenyl ketones has been successfully developedviathe reactions of enynes with radicals enabled by dual photoredox/copper catalysis. Based on the results of a deuteration experiment and the competition reaction between cyclopropanation and allenation, the mechanism based on a photoredox-neutral-catalysed radical-polar crossover process has been proposed. Synthetic applications of allenes have also been demonstrated.

Synthesis and pharmacological evaluation of some new fluorine containing hydroxypyrazolines as potential anticancer and antioxidant agents

Breast cancer is probably the most prevalent cancer in women. The development of resistance to therapeutic agents and lack of targeted therapy for breast cancer cells provide motivation to identify new compounds for the treatment. With this objective in m

GAS-SOLID REACTIONS : PART VI. INTERACTION OF SOLID CHALCONES WITH BROMINE AND IODINE VAPOURS

Solid chalcones (azylidene acetophenones) give, on exposure to bromine vapour at room temperature, the "trans-adduct" in quantitative or near-quantitative yield.Polymorphic forms of several compounds do not differ in their bromination products.Iodine vapours do not cause cis-trans isomerisation in the solid cis-chalcones.