76963-19-4

Basic information

• Product Name: 2-benzyl-2-methyl-1-tetralone
• Synonyms: 2-benzyl-2-methyl-1-tetralone
• CAS NO: 76963-19-4
• Molecular Weight: 250.34
• Mol File: 76963-19-4.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 2-benzyl-2-methyl-1-tetralone(CAS DataBase Reference)
• NIST Chemistry Reference: 2-benzyl-2-methyl-1-tetralone(76963-19-4)
• EPA Substance Registry System: 2-benzyl-2-methyl-1-tetralone(76963-19-4)

Safety Data

• Hazardous Substances Data: 76963-19-4(Hazardous Substances Data)

Upstream product

• 100-39-0 benzyl bromide 
• 74477-40-0 trimethyl(2-methyl-3,4-dihydronaphthalen-1-yloxy)silane 
• 1590-08-5 2-methyl-1-tetralone 

Downstream Products

• 76963-22-9 Thioacetic acid S-((1R,1aS,7bS)-1a-methyl-1-phenyl-1,1a,2,3-tetrahydro-cyclopropa[a]naphthalen-7b-yl) ester 
• 76963-21-8 (1R,1aS,7bS)-1a-Methyl-1-phenyl-1,1a,2,3-tetrahydro-cyclopropa[a]naphthalene-7b-thiol 
• 59530-93-7 2-benzyl-2-methyl-1-thiotetralone 

Relevant articles and documents

Construction of chiral quaternary carbon centers by asymmetric alkylation of achiral lithium enolates mediated by chiral tetradentate ligands: Stoichiometric and catalytic approaches

Enantioselective asymmetric alkylation of achiral lithium enolates mediated by chiral tetradentate amine ligands is achieved to give chiral quaternary carbon centers. Turnover of a chiral tetradentate amine in the presence of an achiral bidentate amine during the reaction is also realized.

Thione photochemistry: Abstraction and cyclization at the β-position of aralkyl thiones from two excited states

Excitation of a series of β-substituted aralkyl thiones either to the S2 (π,π*) state or to the S1 (n,π*) state leads to a formal insertion into the β-position and the formation of cyclopropyl thiols. The mechanisms of intramolecular