77153-27-6

Usage

Uses

Used in Pharmaceutical Synthesis:
3-(3-bromophenyl)-1-(4-chlorophenyl)prop-2-en-1-one is utilized as an intermediate in the synthesis of various pharmaceuticals, leveraging its unique chemical properties to facilitate the creation of diverse medicinal compounds.
Used in Organic Chemistry:
In the field of organic chemistry, 3-(3-bromophenyl)-1-(4-chlorophenyl)prop-2-en-1-one serves as a valuable intermediate for the synthesis of other organic compounds, taking advantage of its reactivity and the presence of bromine and chlorine atoms for a range of chemical reactions.

Upstream product

• 3132-99-8 m-bromobenzoic aldehyde 
• 99-91-2 para-chloroacetophenone 

Downstream Products

• 77153-47-0 (trans)-1-(m-Bromophenyl)-2-(p-chlorophenyl)cyclopropane 
• 77153-46-9 (cis)-1-(m-Bromophenyl)-2-(p-chlorophenyl)cyclopropane 
• 486997-89-1 (2R,3S,4R,6S)-2,6-Bis-(3-bromo-phenyl)-3-(4-chloro-benzoyl)-4-(4-chloro-phenyl)-1-cyano-4-hydroxy-cyclohexanecarboxylic acid ethyl ester 

Relevant academic research and scientific papers

Monitoring the DNA by ruthenium complexes of heterocyclic N,S-donor ligands and evaluation of biological activities

Neutral N,S-donor bidentate ligands have been synthesized and characterized by NMR and IR spectroscopic techniques. The ligands have been used to synthesized ruthenium(II) complexes ([Ru(L1–L6)PPh3)2Cl2/su

Synthesis and biological activity of 3-aryl-5-(3′ -bromo/chlorophenyl)isoxazoles

3-Aryl-5-(3′-bromo/chlorophenyl)isoxazole derivatives (3a-j, 4a-j) have been prepared by condensing 1-aryl-3-(3′-bromo/ chlorophenyl)-2-propen-1-ones (1a-j, 2a-j) with hydroxylamine hydrochloride. Compounds 1a-j, 2a-j have been synthesized by the reaction

Kinetic Study of the Homolytic Brominolysis of 1,2-Diarylcyclopropanes

The rate constants for the photolytic brominolysis of 22 trans-1,2-diarylcyclopropanes in carbon disulfide relative to an internal standard, p-chlorotoluene, have been determined.The products of the brominolysis are 1,3-dibromo-1,3-diarylpropanes.The rate constants range over 5 orders of magnitude, being enhanced by electrondonating substituents on one or both benzene rings.The quantitative size of the substituent effect (ρ) at either involved carbon center is a function of the substituent at the other center.This fact suggests a continuum of transition-state structures with varying degrees of bond breaking and charge separation.