109327-50-6

Basic information

• Product Name: Naphthalene, 1-ethenyl-3,4-dihydro-2-phenyl-
• CAS NO: 109327-50-6
• Molecular Formula: C18H16
• Molecular Weight: 232.325
• Mol File: 109327-50-6.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: Naphthalene, 1-ethenyl-3,4-dihydro-2-phenyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Naphthalene, 1-ethenyl-3,4-dihydro-2-phenyl-(109327-50-6)
• EPA Substance Registry System: Naphthalene, 1-ethenyl-3,4-dihydro-2-phenyl-(109327-50-6)

Safety Data

• Hazardous Substances Data: 109327-50-6(Hazardous Substances Data)

Upstream product

• 529-34-0 3,4-dihydronaphthalene-1(2H)-one 
• 109327-32-4 c-2-chloro-1,2,3,4-tetrahydro-1-phenylnaphthalen-r-1-ol 
• 17215-80-4 2-chloro-1-tetralone 
• 112631-07-9 2-bromo-3,4-dihydro-1-naphthaldehyde 
• 530-93-8 1,2,3,4-tetrahydronaphthalen-2-one 
• 7498-87-5 2-phenyl-3,4-dihydro-2H-naphthalen-1-one 
• 1826-67-1 vinyl magnesium bromide 
• 591-50-4 iodobenzene 
• 112631-06-8 2-bromo-1-ethenyl-3,4-dihydronaphthalene 

Downstream Products

• 18930-97-7 5,6,11,12-tetrahydrochrysene 

Relevant articles and documents

SYNTHESIS OF CHRYSENES AND OTHER a-FUSED PHENANTHRENES BY A PALLADIUM(O) COUPLING-ELECTROCYCLIC RING CLOSURE SEQUENCE

2-Bromo-1-vinyl-3,4-dihydronaphthalene (1a) has been coupled with several vinyl-, aryl-, and heteroaryl-zinc halides in the presence of tetrakis(triphenylphosphine)palladium(O) to give the corresponding 2-vinyl-, 2-aryl-, and 2-heteroaryl-naphthalenes in

An Approach to the Construction of Aromatic Steroids Using Electrocyclic Ring Closure

Methods for the construction of conjugated trienes in which the central double bond is part of a ring system have been investigated. 2-Chloro-3,4-dihydronaphthalen-1(2H)-one is treated with vinyl-lithium reagents to give the alcohols (10) which, when heat