77153-27-6

Basic information

• Product Name: 3-(3-bromophenyl)-1-(4-chlorophenyl)prop-2-en-1-one
• CAS NO: 77153-27-6
• Molecular Formula: C₁₅H₁₀BrClO
• Molecular Weight: 321.5963
• Mol File: 77153-27-6.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 435.4°C at 760 mmHg
• Flash Point: 217.1°C
• Density: 1.475g/cm³
• Vapor Pressure: 8.77E-08mmHg at 25°C
• Refractive Index: 1.652
• CAS DataBase Reference: 3-(3-bromophenyl)-1-(4-chlorophenyl)prop-2-en-1-one(CAS DataBase Reference)
• NIST Chemistry Reference: 3-(3-bromophenyl)-1-(4-chlorophenyl)prop-2-en-1-one(77153-27-6)
• EPA Substance Registry System: 3-(3-bromophenyl)-1-(4-chlorophenyl)prop-2-en-1-one(77153-27-6)

Safety Data

• Hazardous Substances Data: 77153-27-6(Hazardous Substances Data)

Usage

General Description

3-(3-bromophenyl)-1-(4-chlorophenyl)prop-2-en-1-one is an organic compound with the molecular formula C15H10BrClO. It is a chemical that belongs to the group of chalcones, which are compounds with a flavonoid-like structure. This specific compound is a yellow solid with a strong aromatic odor. It is commonly used as an intermediate in the synthesis of pharmaceuticals and other organic compounds due to its versatile chemical properties. The presence of both bromine and chlorine in its structure makes it useful for a variety of chemical reactions and applications in the field of organic chemistry.

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 articles and documents

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

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.