96667-75-3

Basic information

• Product Name: [3-Isopropenyl-1-(toluene-4-sulfonyl)-cyclobutyl]-methanol
• CAS NO: 96667-75-3
• Molecular Weight: 280.388
• Mol File: 96667-75-3.mol

Chemical Properties

• CAS DataBase Reference: [3-Isopropenyl-1-(toluene-4-sulfonyl)-cyclobutyl]-methanol(CAS DataBase Reference)
• NIST Chemistry Reference: [3-Isopropenyl-1-(toluene-4-sulfonyl)-cyclobutyl]-methanol(96667-75-3)
• EPA Substance Registry System: [3-Isopropenyl-1-(toluene-4-sulfonyl)-cyclobutyl]-methanol(96667-75-3)

Safety Data

• Hazardous Substances Data: 96667-75-3(Hazardous Substances Data)

Upstream product

• 96667-34-4 2-[3-(Toluene-4-sulfonyl)-cyclobutyl]-propan-2-ol 
• 96667-20-8 2-[3-(Toluene-4-sulfonyl)-bicyclo[1.1.0]but-1-yl]-propan-2-ol 
• 86537-30-6 1-(p-tolylsulfonyl)bicyclo<1.1.0>butane 
• 50-00-0 formaldehyd 
• 86537-37-3 1-(3-Isopropenyl-cyclobutanesulfonyl)-4-methyl-benzene 
• 86537-38-4 1-(3-Isopropenyl-cyclobutanesulfonyl)-4-methyl-benzene 

Relevant articles and documents

Bridgehead Reactivity, Nucleophilic and Radical Additions, and Lithium Aluminum Hydride Reduction of 1-(Arylsulfonyl)bicyclobutanes: General Access to Substituted, Functionalized Cyclobutanes. Syntheses of (+/-)-Citrilol Acetate, (+/-)-Junionone, and the

A general approach to the synthesis of a wide range of substituted cyclobutane derivatives is based on two specific reactions of 1-(arylsulfonyl)bicyclobutanes (1) and on some general reactions of the bicyclobutane ring systems.One specific cyclobutane fo

CONJUGATE ADDITION OF ORGANOCOPPER REAGENTS TO 1-ARYLSULFONYLBICYCLOBUTANES. SYNTHESIS OF THE RACEMIC FORM OF THE SEX PHEROMONE OF THE CITRUS MEALYBUG, PLANOCOCCUS CITRI (RISSO)

Conjugate addition of organocopper reagents to 1-arylsulfonylbicyclobutanes yields 3-alkyl or alkenyl 1-arylsulfonylcyclobutanes; a synthesis of the sex pheromone of Planococcus citri is based on this reaction.