1370529-58-0

Basic information

• Product Name: C₁₇H₁₈O
• Synonyms: C₁₇H₁₈O
• CAS NO: 1370529-58-0
• Molecular Weight: 238.329
• Mol File: 1370529-58-0.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: C₁₇H₁₈O(CAS DataBase Reference)
• NIST Chemistry Reference: C₁₇H₁₈O(1370529-58-0)
• EPA Substance Registry System: C₁₇H₁₈O(1370529-58-0)

Safety Data

• Hazardous Substances Data: 1370529-58-0(Hazardous Substances Data)

Upstream product

• 91388-35-1 1-formyl-2-(2,2-dimethylethenyl)benzene 
• 6630-33-7 ortho-bromobenzaldehyde 
• 100-52-7 benzaldehyde 
• 91388-25-9 1-bromo-2-(2-methylprop-1-en-1-yl)benzene 

Downstream Products

• 1370529-41-1 C₁₇H₁₆O₂ 
• 61765-22-8 3-hydroxy-2,2-dimethyl-3-phenyl-indan-1-one 

Relevant articles and documents

Cyclization of (2-alkenylphenyl)carbonyl compounds to polycyclic arenes catalyzed by copper(II) trifluoromethanesulfonate or trifluoromethanesulfuric acid

Various polycyclic arenes, such as naphthalenes, tetrahydroantharacenes, tetrahydrotetracenes, dihydropentacenes, and dihydropentaphenes are prepared from 2-alkenylphenyl ketones and aldehydes by the catalytic use of copper(II) trifluoromethanesulfonate (Cu(OTf)2) or trifluoromethanesulfuric acid (TfOH). Copyright

Photochemical studies on aromatic γ,δ-epoxy ketones: Efficient synthesis of benzocyclobutanones and indanones

Irradiation of terminal aromatic γ,δ-epoxy ketones with a 450 W UV lamp led to Norrish type II cyclization/semi-pinacol rearrangement cascade reaction which formed the benzocyclobutanones containing a full-carbon quaternary center, whereas irradiation of substituted aromatic γ,δ-epoxy ketones led to the indanones through a photochemical epoxy rearrangement and 1,5-biradicals cyclization tandem reaction.