61967-11-1

Basic information

• Product Name: Benzenemethanol, a-methyl-a-(1-methyl-2-propenyl)-
• Synonyms: 3-methyl-2-phenylpent-4-en-2-ol
• CAS NO: 61967-11-1
• Molecular Formula: C12H16O
• Molecular Weight: 176.258
• Mol File: 61967-11-1.mol
• Article Data: 35

Chemical Properties

• CAS DataBase Reference: Benzenemethanol, a-methyl-a-(1-methyl-2-propenyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzenemethanol, a-methyl-a-(1-methyl-2-propenyl)-(61967-11-1)
• EPA Substance Registry System: Benzenemethanol, a-methyl-a-(1-methyl-2-propenyl)-(61967-11-1)

Safety Data

• Hazardous Substances Data: 61967-11-1(Hazardous Substances Data)

Upstream product

• 108-94-1 cyclohexanone 
• 6088-87-5 2-butenylmagnesium bromide 
• 98-86-2 acetophenone 
• 66534-82-5 3-tert-butyl-2,2,4-trimethyl-hex-5-en-3-ol 
• 4784-77-4 (E)-1-Bromo-2-butene 
• 98-83-9 isopropenylbenzene 
• 66534-32-5 α,α-diisopropyl-β-methylhomoallylic alcohol 
• 591-97-9 1-chloro-2-butene 
• 106-99-0 buta-1,3-diene 
• 4784-77-4 (E/Z)-crotyl bromide 
• 21969-32-4 (1-methylallyl)magnesium chloride 
• 121725-70-0 but-2-enyl ethyl carbonate 
• 52884-09-0 (2SR,3RS)-3-methyl-2-phenylpent-4-yn-2-ol 
• 702-04-5 crotyl phenyl sulfide 

Downstream Products

• 85312-81-8 (2S^*,3R^*)-3-Hydroxy-2-methyl-3-phenylbutansaeure 
• 34239-38-8 3-hydroxy-2-methyl-3-phenylbutanoic acid 
• 4773-83-5 1,2,3-trimethyl-1H-indene 

Relevant articles and documents

Regio- and stereoselective preparation of highly substituted tertiary homoallylic alcohols

The titanocene(II)-promoted reaction of α-(benzyldimethylsilyl) allylic sulfides with ketones proceeded with high regio- and stereoselectivity to give δ-silylhomoallylic alcohols. The following palladium catalyzed cross-couplings with organic halides prod

Direct use of 1,3-dienes for the allylation of ketones: Via catalytic hydroindation

In this study, in situ catalytically generated allylic indium from 1,3 dienes and InCl2H was developed for use in the allylation of ketones. This protocol resulted in the unprecedented establishment of a successive combining of quaternary C-C b

Synthesis of highly substituted indene derivatives by Br?nsted acid catalyzed Friedel-Crafts reaction of homoallylic alcohols

An efficient synthetic method to prepare highly substituted indenes in moderate to excellent yields that relies on Br?nsted acid catalyzed Friedel-Crafts reaction of homoallylic alcohols under mild conditions is described.