127311-30-2

Basic information

• Product Name: (1R*,2S*,3R*)-6-hydroxy-1-(4-hydroxyphenyl)-2,5,7-trimethyl-3-(2-phenylethyl)-2,3-dihydroindene
• CAS NO: 127311-30-2
• Molecular Weight: 372.507
• Mol File: 127311-30-2.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: (1R*,2S*,3R*)-6-hydroxy-1-(4-hydroxyphenyl)-2,5,7-trimethyl-3-(2-phenylethyl)-2,3-dihydroindene(CAS DataBase Reference)
• NIST Chemistry Reference: (1R*,2S*,3R*)-6-hydroxy-1-(4-hydroxyphenyl)-2,5,7-trimethyl-3-(2-phenylethyl)-2,3-dihydroindene(127311-30-2)
• EPA Substance Registry System: (1R*,2S*,3R*)-6-hydroxy-1-(4-hydroxyphenyl)-2,5,7-trimethyl-3-(2-phenylethyl)-2,3-dihydroindene(127311-30-2)

Safety Data

• Hazardous Substances Data: 127311-30-2(Hazardous Substances Data)

Upstream product

• 127311-26-6 2,6-dimethyl-4-(3-phenylpropyl)phenol 
• 127311-27-7 2,6-Dimethyl-4-<(3-phenyl)propylidene>-2,5-cyclohexadien-1-one 
• 539-12-8 (Z)-1-(4-hydroxyphenyl)propene 

Relevant articles and documents

Formal Cycloaddition of Benzylic Cations with Alkenes

The reaction of benzylic cations with styrenes affords dihydro(1H)indenes in good yield via a formal atom cycloadditon.The cations were generated from quinone methides and benzylic alcohols. (E)-Styrenes participate in the reaction with remarkable stereoselectivity affording dihydro(1H)indenes with three stereogenic centers with >40:1 diastereoselectivity.A possible transition state for the reaction is discussed.Less activated alkenes such as dihydropyran and methylcyclohexane afforded cycloadducts in 66percent and 51percent yields, respectively.