55359-62-1

Basic information

• Product Name: 5-methoxy-2-phenyl-2,3-dihydro-1H-inden-1-one
• Synonyms: 5-methoxy-2-phenyl-2,3-dihydro-1H-inden-1-one
• CAS NO: 55359-62-1
• Molecular Weight: 238.286
• Mol File: 55359-62-1.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 5-methoxy-2-phenyl-2,3-dihydro-1H-inden-1-one(CAS DataBase Reference)
• NIST Chemistry Reference: 5-methoxy-2-phenyl-2,3-dihydro-1H-inden-1-one(55359-62-1)
• EPA Substance Registry System: 5-methoxy-2-phenyl-2,3-dihydro-1H-inden-1-one(55359-62-1)

Safety Data

• Hazardous Substances Data: 55359-62-1(Hazardous Substances Data)

Upstream product

• 82632-40-4 5-methoxy-trans-stilbene-2-carbaldehyde 
• 824-98-6 m-methoxybenzyl chloride 
• 103-82-2 phenylacetic acid 
• 24298-04-2 (E)-α-(3'-methoxyphenylmethylene)benzeneacetic acid 
• 103-80-0 phenylacetyl chloride 
• 100-66-3 methoxybenzene 
• 1023-17-2 4-methoxyphenyl benzyl ketone 
• 93300-81-3 β-(m-methoxyphenyl)-α-phenylpropionic acid 

Downstream Products

• 988-43-2 4-{2-[4-(5-methoxy-2-phenyl-3H-inden-1-yl)-phenoxy]-ethyl}-morpholine 
• 345622-67-5 1,2-cis/trans-2-phenyl-5-methoxy-1-indanol 
• 912-63-0 3-<4-(2-Diaethylamino-aethoxy)-phenyl>-6-hydroxy-2-phenyl-inden 
• 78014-13-8 2-phenyl-5-methoxyindane 
• 78014-12-7 6-methoxyl-2-phenyl-1H-indene 
• 102345-53-9 3-<4-(2-Diaethylamino-aethoxy)-phenyl>-5-methoxy-2-phenyl-inden 

Relevant articles and documents

Rhodium-catalyzed intramolecular hydroacylation of 1,2-disubstituted alkenes for the synthesis of 2-substituted indanones

The intramolecular hydroacylation of 1,2-disubstituted alkenes was considered to be a challenging task due to the side reactions resulted from the lack of additional substituent at 1-position and the low activity caused by the steric hindrance of substituent at 2-position, and an asymmetric version has not been considered possible due to problems associated with the racemization of the products. We have partially solved these problems. Catalyzed by an activated diphosphine-Rh complex and reacted in a selected dihalogenated solvent, the intramolecular hydroacylation of o-(2-arylvinyl)benzaldehydes provided the corresponding 2-aryl-1-indanones in high yields, and its asymmetric variant using o-(2-alkylvinyl)benzaldehydes afforded chiral 2-alkyl-1-indanones in high yields and with moderate enantioselectivities.

Preparation of carbon-14 labeled 2-phenyl-3-[p-(2-diethylaminoethoxy) phenyl]-6-methoxyindene hydrochloride

-