55223-24-0

Basic information

• Product Name: 1H-Inden-1-one, 2-[(2-bromophenyl)methyl]-2,3-dihydro-
• CAS NO: 55223-24-0
• Molecular Formula: C16H13BrO
• Molecular Weight: 301.183
• Mol File: 55223-24-0.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: 1H-Inden-1-one, 2-[(2-bromophenyl)methyl]-2,3-dihydro-(CAS DataBase Reference)
• NIST Chemistry Reference: 1H-Inden-1-one, 2-[(2-bromophenyl)methyl]-2,3-dihydro-(55223-24-0)
• EPA Substance Registry System: 1H-Inden-1-one, 2-[(2-bromophenyl)methyl]-2,3-dihydro-(55223-24-0)

Safety Data

• Hazardous Substances Data: 55223-24-0(Hazardous Substances Data)

Upstream product

• 83-33-0 inden-1-one 
• 6630-33-7 ortho-bromobenzaldehyde 
• 1352732-72-9 (E)-2,2'-(prop-1-ene-1,3-diyl)bis(bromobenzene) 
• 2142-69-0 2-bromophenyl methyl ketone 
• 3433-80-5 1-Bromo-2-bromomethyl-benzene 
• 103457-38-1 (E)-2-(2-bromobenzylidene)-2,3-dihydro-1H-inden-1-one 

Downstream Products

• 278780-91-9 3-(2-bromophenyl)-1,2-naphthoquinone 
• 278780-87-3 3-(2-bromophenyl)naphthalen-2-ol 
• 278780-85-1 2-[3-(2-bromophenyl)-2-oxopropyl]benzaldehyde 
• 278780-83-9 2-(2-bromobenzyl)-1H-indene 
• 278780-93-1 2-(2-bromophenyl)-3-hydroxy-1,4-naphthoquinone 
• 479-11-8 benzo[b]naphtho[2,3-d]furan-6,11-dione 
• 243-42-5 β-brazan 

Relevant articles and documents

Iridium-catalyzed chemoselective transfer hydrogenation of α, β-unsaturated ketones to saturated ketones in water

A chemoselective iridium-catalyzed transfer hydrogenation of α, β-unsaturated ketones was realized in water. The C[dbnd]C double bonds of 2-benzylidene indanones and analogues were hydrogenated exclusively catalyzed by an iridium complex (0.1 mol%) bearin

PYRIDOPYRAZINE AND PYRIDOTRIAZINE INHIBITORS OF INFLUENZA VIRUS REPLICATION

Provided herein are compounds that can inhibit the replication of influenza viruses, reduce the amount of influenza viruses, and/or treat influenza. (I)

Radical cyclisation onto nitriles

Iminyl radicals, generated by 5-exo cyclisation of alkyl, vinyl and aryl C-centred radicals onto nitriles, undergo β-scission (nitrile translocation), reduction or tandem cyclisation onto alkenes depending on the nature of the α-substituent. 5-exo Cyclisations of aryl radicals onto nitriles undergo nitrile translocation when the α-substituent is CN, CO2R, SO2Ph or CONMe2. The rate of translocation is faster than 5- or 6-exo cyclisation onto alkenes or 1,5-hydrogen abstraction of allylic hydrogens. When the α-substituents are alkyl, the intermediate iminyl radicals do not undergo nitrile translocation. (C) 2000 Elsevier Science Ltd.