62901-82-0

Basic information

• Product Name: Benzeneacetic acid, a-3-butenyl-a-phenyl-
• CAS NO: 62901-82-0
• Molecular Formula: C18H18O2
• Molecular Weight: 266.34
• Mol File: 62901-82-0.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: Benzeneacetic acid, a-3-butenyl-a-phenyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzeneacetic acid, a-3-butenyl-a-phenyl-(62901-82-0)
• EPA Substance Registry System: Benzeneacetic acid, a-3-butenyl-a-phenyl-(62901-82-0)

Safety Data

• Hazardous Substances Data: 62901-82-0(Hazardous Substances Data)

Upstream product

• 530-48-3 1,1-Diphenylethylene 
• 124-38-9 carbon dioxide 
• 3052-45-7 allyllithium 
• 117-34-0 2,2-diphenylacetic acid 
• 3469-00-9 methyl 2,2-diphenylacetate 
• 752207-03-7 2,2-diphenylhex-5-enoic acid methyl ester 
• 109-72-8 n-butyllithium 

Downstream Products

• 1912-08-9 5-methyl-2,2-diphenylcyclopentan-1-one 
• 73982-28-2 6,6-diphenylcyclohex-2-en-1-one 
• 141536-27-8 <(2',2'-diphenyl-4'-methylenecyclopropyl)butoxythiocarbonyl>-1-imidazole 
• 167300-32-5 (2,2-diphenyl-4-methylenecyclopropyl)butyl methanesulphonate 
• 167300-31-4 2-<2',2'-diphenyl-4'-(methylenecyclopropyl)butoxy>tetrahydropyran 
• 141536-28-9 (2,2-diphenyl-4-methylenecyclopropyl)butyl phenyl selenide 
• 141536-25-6 2-(2',2'-diphenyl-5'-hexenyloxy)tetrahydropyran 
• 141536-26-7 2,2-diphenyl-4-methylenecyclopropylbutan-1-ol 
• 167300-48-3 2,2-diphenyl-5-hexen-1-ol 
• 95280-10-7 5-Oxo-2,2-diphenyl-valeriansaeure 

Relevant articles and documents

Enantio- and Regioselective Palladium(II)-Catalyzed Dioxygenation of (Aza-)Alkenols

An oxidative Pd-catalyzed intra-intermolecular dioxygenation of (aza-)alkenols has been reported, with total regioselectivity. To study the stereoselectivity, different chiral ligands as well as different hypervalent-iodine compounds have been compared. I

Cobalt-catalyzed cyclization with the introduction of cyano, acyl and aminoalkyl groups

An efficient synthesis of carbo-and heterocycles using CC, CO and CN bonds under cobalt catalysis is described. The substituents on olefins are key for controlling the regio-and chemoselectivity in the initial hydrogen atom transfer step and quaternary carbons are efficiently constructed under mild conditions. Cyclopropane cleavage and tandem cyclization give highly functionalized bicyclic skeletons in a single operation.