61592-98-1

Basic information

• Product Name: Ethanone, 1,2-bis(2-bromophenyl)-2-hydroxy-
• CAS NO: 61592-98-1
• Molecular Formula: C14H10Br2O2
• Molecular Weight: 370.04
• Mol File: 61592-98-1.mol
• Article Data: 7

Chemical Properties

• Melting Point: 76-78 °C
• Boiling Point: 464.8±40.0 °C(Predicted)
• Density: 1.743±0.06 g/cm3(Predicted)
• CAS DataBase Reference: Ethanone, 1,2-bis(2-bromophenyl)-2-hydroxy-(CAS DataBase Reference)
• NIST Chemistry Reference: Ethanone, 1,2-bis(2-bromophenyl)-2-hydroxy-(61592-98-1)
• EPA Substance Registry System: Ethanone, 1,2-bis(2-bromophenyl)-2-hydroxy-(61592-98-1)

Safety Data

• Hazardous Substances Data: 61592-98-1(Hazardous Substances Data)

Usage

General Description

Ethanone, 1,2-bis(2-bromophenyl)-2-hydroxy- is a chemical compound with the molecular formula C14H10Br2O2. It is a derivative of acetophenone and contains two bromine atoms and one hydroxy group. Ethanone, 1,2-bis(2-bromophenyl)-2-hydroxy- is mainly used in organic synthesis and pharmaceutical research. Its properties and uses are still being studied, but it has potential applications in the development of new drugs and other organic compounds. As with any chemical compound, proper handling and safety precautions should be taken when working with it.

Upstream product

• 78-84-2 isobutyraldehyde 
• 6630-33-7 ortho-bromobenzaldehyde 
• 104-53-0 3-phenyl-propionaldehyde 

Downstream Products

• 25187-01-3 2,2’-dibromobenzophenone 
• 61592-89-0 2,2’-dibromodiphenylmethane 
• 1159711-20-2 1,2-bis[(2-bromophenyl)]-2-chloroethanone 
• 7433-92-3 ⁽²⁾-benzopyrano(4,3-c)-⁽²⁾benzopyrano-6,12-dione 
• 19357-64-3 Biphthalidyliden 
• 172277-05-3 (1RS,2SR)-1,2-bis(2-bromophenyl)ethane-1,2-diol 
• 63818-44-0 2,2'-Dibrombenzil-dimethylmonoketal 
• 51417-57-3 1,2-Bis(2-bromophenyl)ethane-1,2-dione 
• 123335-02-4 bis-(2-bromophenyl)methanol 

Relevant articles and documents

Palladium-Catalyzed Double Carbonylative Cyclization of Benzoins: Synthesis and Photoluminescence of Bis-Ester-Bridged Stilbenes

A palladium-catalyzed double carbonylative cyclization of benzoins has been developed, which realizes the synthesis of bis-ester-bridged stilbenes just in two steps from aldehydes. Thus, the obtained fully fused tetracyclic π-systems have a pyrano[3,2-b]pyran-2,6-dione (PPD) core on their center, showing two reversible reductions at low potentials. In addition, their photoluminescence properties are strikingly affected by the aromatic rings fused to the PPD core; bis-thieno-fused PPDs are found to be excellent fluorophores with quantum yields up to 0.98.

Chemoselective and repetitive intermolecular cross-acyloin condensation reactions between a variety of aromatic and aliphatic aldehydes using a robust N-heterocyclic carbene catalyst

We found that chemoselectivity of the crossed acyloin product is controlled by the adjustment of the aromatic aldehyde/aliphatic aldehyde ratio. Moreover, we observed the persistent catalytic activity of the homogeneous NHC catalyst in a solution due to N

Synthesis and photoreactivity of aryl substituted 4,5-dithienyl[1,3]dithiol-2-ones

UV irradiation of hitherto unknown 4,5-bis-benzo[b]thiophen-3-yl-[1,3]dithiol-2-one gave 3-(3-benzo[b]thienyl)-thieno[3,4-c]benzo[e][1,2]dithiine by loss of carbon monoxide and rearrangement, whereas 4,5-bis-(2-bromo-phenyl)-[1,3]dithiol-2-one gave a poly