32045-79-7

Usage

Type of compound

Ketone derivative

Structural features

Biphenyl-4-yl group
Two bromine atoms attached to the 2 and 3 positions of the propan-1-one chain
Phenyl group attached to the 3 position

Applications

Organic synthesis
Pharmaceutical research

Unique properties

Aromatic features
Halogenated features

Importance in synthesis

Valuable building block for various organic compounds

Potential

Pharmacological properties for drug development and discovery

Safety precautions

Follow proper safety protocols and procedures due to potentially hazardous nature

Upstream product

• 100-52-7 benzaldehyde 
• 92-91-1 biphenyl-4-acetaldehyde 
• 81878-54-8 1-biphenyl-4'-yl-3-phenylprop-2-enone 

Downstream Products

• 51813-19-5 3-([1,1'-biphenyl]-4-yl)-5-phenylisoxazole 
• 7464-89-3 1,3,6,8-tetramethyl-1H,3H,6H,8H-pyrimido[4,5-g]pteridine-2,4,7,9-tetraone 
• 37974-77-9 1-[(1,1′-biphenyl)-4-yl]-3-phenylpropane-1,3-dione 
• 857229-09-5 1-(biphenyl-4-yl)-2,3-di(morpholin-4-yl)-3-phenylpropan-1-one 
• 96872-64-9 1,4-Bis-(p-biphenylyl)-2,3-dibenzoyl-butan-1,4-dion 

Relevant academic research and scientific papers

Synthesis and antimicrobial evaluation of some halcones and their derived pyrazoles, pyrazolines, isoxazolines, and 5,6-dihydropyrimidine-2-(1H)-thiones

Chalcones were synthesized by a base catalyzed Claisen-Schmidt condensation reaction. Bromination of chalcones afforded the dibromo derivatives. Monobromo derivatives could be obtained by treating the corresponding dibromochalcones with dry benzene in the

Diaroyl(methanato)boron Difluoride Compounds as Medium-Sensitive Two-Photon Fluorescent Probes

This paper evaluates the use of diaroyl(methanato)boron difluoride compounds for designing efficient fluorescent probes through two-photon absorption. Three different pathways allowing for the syntheses of symmetrical and dissymmetrical molecules are reported. The stable diaroyl(methanato)-boron difluoride derivatives can be easily obtained in good yields. They exhibit a large one-photon absorption that is easily tuned in the near-UV range. Their strong fluorescence emission covers the whole visible domain. In addition to these attractive linear properties, several diaroyl(methanato)-boron difluoride derivatives possess significant cross sections for two-photon absorption. The derived structure-property relationships are promising for designing new generations of molecules relying on the diaroyl(methanato)boron difluoride backbone.