161065-36-7

Basic information

• Product Name: Ethanone, 2,2-bis(octyloxy)-1-phenyl-
• CAS NO: 161065-36-7
• Molecular Formula: C24H40O3
• Molecular Weight: 376.58
• Mol File: 161065-36-7.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: Ethanone, 2,2-bis(octyloxy)-1-phenyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Ethanone, 2,2-bis(octyloxy)-1-phenyl-(161065-36-7)
• EPA Substance Registry System: Ethanone, 2,2-bis(octyloxy)-1-phenyl-(161065-36-7)

Safety Data

• Hazardous Substances Data: 161065-36-7(Hazardous Substances Data)

Upstream product

• 111-87-5 octanol 
• 1074-12-0 phenylglyoxal hydrate 
• 98-86-2 acetophenone 

Downstream Products

• 586398-13-2 3,3-bis-octyloxy-2-phenyl-2-trimethylsilanyloxy-propionitrile 

Relevant articles and documents

Synergistic Catalysis of Se and Cu for the Activation of α-H of Methyl Ketones with Molecular Oxygen/Alcohol to Produce α-Keto Acetals?

Selenium and copper synergistically catalyzed the oxidation/alkoxylation of methyl ketones to synthesize α-keto acetals directly. Using O2 as oxidant and alcohol as solvent and alkoxylation reagent, the reaction is practical from industrial viewpoint. Mechanistic studies revealed that copper promoted the oxidation of organoselenium intermediates with O2 to allow the key rearrangement and selenoxide syn-elimination regenerating the catalytically active organoselenium species.

Catalytic asymmetric cyanosilylation of ketones, aldehydes, thioketones, thioaldehydes, imines and hydrazones

One aspect of the present invention relates to a method for the catalytic asymmetric cyanosilylation of ketones, aldehydes, thioketones, thioaldehydes, imines and hydrazones. The critical elements of the method are: a non-racemic chiral tertiary-amine-con