1439386-58-9

Basic information

• Product Name: 1-(4-(tert-butyl)benzyl)cyclopropanol
• Synonyms: 1-(4-(tert-butyl)benzyl)cyclopropanol
• CAS NO: 1439386-58-9
• Molecular Weight: 204.312
• Mol File: 1439386-58-9.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 1-(4-(tert-butyl)benzyl)cyclopropanol(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(4-(tert-butyl)benzyl)cyclopropanol(1439386-58-9)
• EPA Substance Registry System: 1-(4-(tert-butyl)benzyl)cyclopropanol(1439386-58-9)

Safety Data

• Hazardous Substances Data: 1439386-58-9(Hazardous Substances Data)

Upstream product

• 14062-22-7 ethyl 2-(4-(tert-butyl)phenyl)acetate 
• 925-90-6 ethylmagnesium bromide 
• 3549-23-3 methyl 2-(4-tert-butylphenyl)acetate 

Downstream Products

• 1439386-81-8 C₂₂H₂₄OS 
• 1439386-80-7 C₂₇H₃₃NO₃ 
• 1439386-79-4 C₁₉H₂₄OS 
• 1439386-78-3 C₁₉H₂₃NO 
• 1439386-77-2 C₂₆H₃₅NO₃ 
• 1439386-75-0 C₂₅H₂₈O₂ 

Relevant articles and documents

Ni-Catalyzed Denitrogenative Cross-Coupling of Benzotriazinones and Cyclopropanols: An Easy Access to Functionalized β-Aryl Ketones

A novel Ni-catalyzed denitrogenative cross-coupling between benzotriazinones and cyclopropanols is reported herein. This neoteric reactivity allows for the convenient synthesis of β-(o-amido)aryl ketones from readily available starting materials with good yields (up to 93percent) and general substrate scope.

Palladium-catalyzed cross-coupling of cyclopropanol-derived ketone homoenolates with aryl bromides

The cross-coupling reaction of cyclopropanol-derived ketone homoenolates bearing β-hydrogens with aryl and hetaryl bromides has been achieved for the first time. This reaction is high yielding, is broad in scope and uses a simple catalytic system. Notably, the proposed palladium homoenolates do not undergo β-hydride elimination to the corresponding α,β- unsaturated ketones.