106116-47-6

Basic information

• Product Name: 2-(3,5-Dimethoxybenzyl)-2-(3,5-dimethylbenzyl)-2,3-dihydro-5,7-dimethoxy-1H-inden-1-on
• CAS NO: 106116-47-6
• Molecular Weight: 460.57
• Mol File: 106116-47-6.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 2-(3,5-Dimethoxybenzyl)-2-(3,5-dimethylbenzyl)-2,3-dihydro-5,7-dimethoxy-1H-inden-1-on(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(3,5-Dimethoxybenzyl)-2-(3,5-dimethylbenzyl)-2,3-dihydro-5,7-dimethoxy-1H-inden-1-on(106116-47-6)
• EPA Substance Registry System: 2-(3,5-Dimethoxybenzyl)-2-(3,5-dimethylbenzyl)-2,3-dihydro-5,7-dimethoxy-1H-inden-1-on(106116-47-6)

Safety Data

• Hazardous Substances Data: 106116-47-6(Hazardous Substances Data)

Upstream product

• 106116-39-6 2-(3,5-Dimethoxybenzyliden)-2,3-dihydro-5,7-dimethoxy-1H-inden-1-on 
• 880-87-5 5,7-dimethoxyindan-1-one 
• 7311-34-4 3,5-dimethoxybenzaldehdye 
• 27129-86-8 1-bromomethyl-3,5-dimethylbenzene 
• 106116-43-2 2-(3,5-Dimethoxybenzyl)-2,3-dihydro-5,7-dimethoxy-1H-inden-1-on 

Relevant articles and documents

Benzoannelated Centropolyquinanes, 3. - Synthesis of Multiply Substituted Triptindans (9H,10H-4b,9a-(Benzenomethano)indenoindenes) with Substituents in their Molecular Cavity

The synthesis of triptindans 13a-e substituted by methoxy and/or methyl groups in positions 2,4,5,7,13, and 15 has been achieved by acid-catalysed cyclodehydration of the corresponding 2,2-dibenzyl-1-indanones 12a-e using Amberlyst 15 and polyphosphoric acid, respectively.Total demethylation of 13a followed by selective deoxygenation of the resulting hexahydroxy compound 14 affords the 4,5,15-trihydroxytriptindan (17) (4, R = OH) bearing the three substituents in its molecular cavity.