99547-48-5

Basic information

• Product Name: 2-(3,4-dihydroisoquinolin-2(1H)-yl)-1-phenylpropan-1-one
• Synonyms: 2-(3,4-dihydroisoquinolin-2(1H)-yl)-1-phenylpropan-1-one
• CAS NO: 99547-48-5
• Molecular Weight: 265.355
• Mol File: 99547-48-5.mol
• Article Data: 7

Chemical Properties

• CAS DataBase Reference: 2-(3,4-dihydroisoquinolin-2(1H)-yl)-1-phenylpropan-1-one(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(3,4-dihydroisoquinolin-2(1H)-yl)-1-phenylpropan-1-one(99547-48-5)
• EPA Substance Registry System: 2-(3,4-dihydroisoquinolin-2(1H)-yl)-1-phenylpropan-1-one(99547-48-5)

Safety Data

• Hazardous Substances Data: 99547-48-5(Hazardous Substances Data)

Upstream product

• 91-21-4 1,2,3,4-tetrahydroisoquinoline 
• 93-55-0 1-phenyl-propan-1-one 
• 93-54-9 1-Phenyl-1-propanol 
• 108-86-1 bromobenzene 
• 4393-06-0 1-Phenyl-2-propen-1-ol 
• 2114-00-3 2-bromo-1-phenyl-1-propanone 

Relevant articles and documents

Synthesis of α-Iodoketones from Allylic Alcohols through Aerobic Oxidative Iodination

An efficient method for the synthesis of α-iodoketones from allylic alcohols and elemental iodine is reported. We show in this paper that the isomerization of allylic alcohols catalyzed by iridium(III) complexes can be combined with an aerobic oxidative iodination protocol, resulting in a straightforward method for the synthesis of a wide range of α-iodoketones as single constitutional isomers and in high yields under mild reaction conditions. (Figure presented.).

Electrochemically Oxidative α-C-H Functionalization of Ketones: A Cascade Synthesis of α-Amino Ketones Mediated by NH4I

An efficient electrochemical protocol for the synthesis of α-amino ketones via the oxidative cross-dehydrogenative coupling of ketones and secondary amines has been developed. The electrochemistry performs in a simple undivided cell using NH4I

Synthesis and characterization of bisoxazolines- and pybox-copper(II) complexes and their application in the coupling of α-carbonyls with functionalized amines

Binuclear complexes [{(DMOX)CuCl}2(μ-Cl)2] (1), mononuclear complexes [(DMOX)CuBr2] (2) (DMOX = 4,5-dihydro-2-(4,5- dihydro-4,4-dimethyloxazol-2-yl)-4,4-dimethyloxazole) and the pybox Cu(ii) complex [(Dm-Pybox)CuBr2/