32565-73-4

Basic information

• Product Name: 1H-Inden-5-ol, 2,3-dihydro-3-(4-hydroxy-3,5-dimethylphenyl)-1,1,3,4,6-pentamethyl-
• CAS NO: 32565-73-4
• Molecular Formula: C22H28O2
• Molecular Weight: 324.463
• Mol File: 32565-73-4.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 1H-Inden-5-ol, 2,3-dihydro-3-(4-hydroxy-3,5-dimethylphenyl)-1,1,3,4,6-pentamethyl-(CAS DataBase Reference)
• NIST Chemistry Reference: 1H-Inden-5-ol, 2,3-dihydro-3-(4-hydroxy-3,5-dimethylphenyl)-1,1,3,4,6-pentamethyl-(32565-73-4)
• EPA Substance Registry System: 1H-Inden-5-ol, 2,3-dihydro-3-(4-hydroxy-3,5-dimethylphenyl)-1,1,3,4,6-pentamethyl-(32565-73-4)

Safety Data

• Hazardous Substances Data: 32565-73-4(Hazardous Substances Data)

Upstream product

• 55182-63-3 4‐(2‐hydroxypropan‐2‐yl)‐2,6‐dimethylphenol 
• 5613-46-7 tetramethylbisphenol A 
• 32565-69-8 2.6-Dimethyl-4-isopropenyl-phenol 

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.