119612-35-0

Basic information

• Product Name: 1β-Benzoyl-1aβ,2,3,7bβ-tetrahydrocyclopropanaphthalene
• Synonyms: 1β-Benzoyl-1aβ,2,3,7bβ-tetrahydrocyclopropanaphthalene
• CAS NO: 119612-35-0
• Molecular Weight: 248.324
• Mol File: 119612-35-0.mol

Chemical Properties

• CAS DataBase Reference: 1β-Benzoyl-1aβ,2,3,7bβ-tetrahydrocyclopropanaphthalene(CAS DataBase Reference)
• NIST Chemistry Reference: 1β-Benzoyl-1aβ,2,3,7bβ-tetrahydrocyclopropanaphthalene(119612-35-0)
• EPA Substance Registry System: 1β-Benzoyl-1aβ,2,3,7bβ-tetrahydrocyclopropanaphthalene(119612-35-0)

Upstream product

• 447-53-0 1,2-Dihydronaphthalene 
• 3282-32-4 2-diazo-acetophenone 

Downstream Products

• 119612-41-8 5-<2'(1'-Bromo-1',2',3',4'-tetrahydro)naphthyl>-4-phenyl-1,4-pentadiene 

Relevant articles and documents

Tetrahydrothiophene-catalyzed synthesis of benzo[n.1.0] bicycloalkanes

(Chemical Equation Presented) A catalytic intramolecular cyclopropanation for the preparation of benzobicyclic compounds with [n.1.0] units has been developed. In the presence of 20 mol % of tetrahydrothiophene, the reactions of compounds 2a-2h afford ver

Reactions of α-Diazoketones with Olefinic Compounds in Presence of Catalysts and Related Studies

A relatively stable cyclopropane adduct is produced by trapping ketocarbenes in olefin.The reactivities of ketocarbenes prepared thermally from different α-diazoketones and of the olefin substrates, and the effect of different catalysts and solvents are some of the parameters which have a pronounced effect on the yield of the products.Besides the cyclopropane adducts some side products have also been isolated and characterized.