82315-88-6

Basic information

• Product Name: 2-Butanone, 1-(2-cyclohexen-1-yl)-3,3-dimethyl-
• CAS NO: 82315-88-6
• Molecular Formula: C12H20O
• Molecular Weight: 180.29
• Mol File: 82315-88-6.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 2-Butanone, 1-(2-cyclohexen-1-yl)-3,3-dimethyl-(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Butanone, 1-(2-cyclohexen-1-yl)-3,3-dimethyl-(82315-88-6)
• EPA Substance Registry System: 2-Butanone, 1-(2-cyclohexen-1-yl)-3,3-dimethyl-(82315-88-6)

Safety Data

• Hazardous Substances Data: 82315-88-6(Hazardous Substances Data)

Upstream product

• 1521-51-3 rac-3-bromocyclohexene 
• 17094-34-7 ethyl pivaloylacetate 
• 76644-52-5 rac-3-acetoxycyclohexene 
• 17510-46-2 3,3-dimethyl-2-(trimethylsilyl)oxy-1-butene 

Downstream Products

• 82700-05-8 2-(cyclohex-2-en-1-yl)acetonitrile 

Relevant articles and documents

Highly efficient Narasaka-Heck cyclizations mediated by P(3,5-(CF 3)2C6H3)3: Facile access to N-heterobicyclic scaffolds

N-heterobicyclic scaffolds: Highly efficient palladium-catalyzed cyclizations of oxime esters with cyclic alkenes were used as a general entry to perhydroindole and related scaffolds. The chemistry is reliant upon the use of P(3,5-(CF3)2/

Regioselective Lewis Acid-mediated α-sec-Alkylation of Carbonyl Compounds

Carbonyl compounds such as ketones, aldehydes, acyloins, or carboxylic esters can be alkylated at the α-position via the corresponding O-silylated forms using activated alkyl halides or acetates in the presence of Lewis acids.In the case of unsymmetricall