6271-51-8

Basic information

• Product Name: 2,3-dibromo-1-(4-bromophenyl)-3-phenylpropan-1-one
• CAS NO: 6271-51-8
• Molecular Formula: C₁₅H₁₁Br₃O
• Molecular Weight: 446.9592
• Mol File: 6271-51-8.mol
• Article Data: 6

Chemical Properties

• Boiling Point: 466.4°C at 760 mmHg
• Flash Point: 120.5°C
• Density: 1.848g/cm³
• Vapor Pressure: 7.11E-09mmHg at 25°C
• Refractive Index: 1.652
• CAS DataBase Reference: 2,3-dibromo-1-(4-bromophenyl)-3-phenylpropan-1-one(CAS DataBase Reference)
• NIST Chemistry Reference: 2,3-dibromo-1-(4-bromophenyl)-3-phenylpropan-1-one(6271-51-8)
• EPA Substance Registry System: 2,3-dibromo-1-(4-bromophenyl)-3-phenylpropan-1-one(6271-51-8)

Safety Data

• Hazardous Substances Data: 6271-51-8(Hazardous Substances Data)

Usage

General Description

2,3-dibromo-1-(4-bromophenyl)-3-phenylpropan-1-one is a chemical compound with the molecular formula C15H10Br2O. It is a yellow crystalline solid that is commonly used in organic synthesis and pharmacological research. The compound is known for its potent antimicrobial and anticancer properties and has been studied for its potential applications in drug development. Its structural arrangement includes a bromine group, a phenyl group, and a ketone group, making it a versatile compound with various potential uses in the fields of medicine and biotechnology.

Upstream product

• 2403-27-2 1-(4-bromophenyl)-3-phenyl-2-propen-1-one 
• 56-23-5 tetrachloromethane 
• 72758-69-1 (E)-1-(4-bromophenyl)-3-phenylprop-2-en-1-one 
• 64-19-7 acetic acid 

Downstream Products

• 53573-21-0 3-(4-bromophenyl)-5-phenylisoxazole 
• 7464-89-3 1,3,6,8-tetramethyl-1H,3H,6H,8H-pyrimido[4,5-g]pteridine-2,4,7,9-tetraone 
• 117836-59-6 2-(4-Bromo-phenyl)-1-phenyl-1,1a-dihydro-3,7b-diaza-cyclopropa[a]naphthalene-5-carbonitrile 
• 117836-46-1 2-(4-Bromo-phenyl)-1-phenyl-1,1a-dihydro-3,7b-diaza-cyclopropa[a]naphthalene 
• 117836-52-9 5-Bromo-2-(4-bromo-phenyl)-1-phenyl-1,1a-dihydro-3,7b-diaza-cyclopropa[a]naphthalene 
• 127019-13-0 4-(4-Bromo-phenyl)-6-phenyl-1,3-diaza-bicyclo[3.1.0]hex-3-ene 
• 93944-86-6 2-bromo-1-(4-bromophenyl)-3-phenyl-1,3-propanedione 
• 117836-63-2 2-benzyl-3-(4-bromo-phenyl)-quinoxaline 
• 117836-65-4 2-Benzyl-6-bromo-3-(4-bromo-phenyl)-quinoxaline 
• 911678-04-1 1-(4-(4-bromophenyl)-6-phenylpyrimidin-2-yl)hydrazine-1-carbonitrile 

Relevant articles and documents

A one-pot and three-component synthetic approach for the preparation of asymmetric and multi-substituted 1,4-dihydropyrazines

An efficient, one-pot and three-component synthesis of a new series of 2-acyl-3,4,6-triaryl-1,4-dihydropyrazines is described. This two-step strategy involves treatment of phenacyl bromides and anilines to give the nucleophilic substitution intermediate f

I2O5-mediated bromohydroxylation and dibromination of olefins using KBr in water

An efficient and green bromohydroxylation and dibromination of various olefins mediated by I2O5 has been developed in this work. A series of olefins gave the corresponding α-bromo-alcohols and dibromides as the major products using KBr as the brominating reagent in aqueous medium at room temperature. The diastereo- and regio-selectivities are extremely high.

Process for preparing vinyl substituted beta-diketones

A process for preparing vinyl substituted beta-diketones includes reacting a halogen-containing beta-diketone with an olefin in a reaction zone under Heck coupling reaction conditions in the presence of a catalyst, a base, and an organic phosphine to provide a vinyl substituted beta-diketone product.