78427-96-0

Basic information

• Product Name: 4-Octanone, 1-phenyl-
• CAS NO: 78427-96-0
• Molecular Formula: C14H20O
• Molecular Weight: 204.312
• Mol File: 78427-96-0.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 4-Octanone, 1-phenyl-(CAS DataBase Reference)
• NIST Chemistry Reference: 4-Octanone, 1-phenyl-(78427-96-0)
• EPA Substance Registry System: 4-Octanone, 1-phenyl-(78427-96-0)

Safety Data

• Hazardous Substances Data: 78427-96-0(Hazardous Substances Data)

Upstream product

• 542-69-8 1-iodo-butane 
• 72863-31-1 2-pyridyl 4-phenylbutanoate 
• 78427-97-1 4-Phenyl-butyric acid 6-methyl-pyridin-2-yl ester 
• 78427-99-3 2-(6-(2-methoxyethyl)pyridyl) 4-phenylbutanoate 
• 78428-01-0 4-Phenyl-butyric acid 6-(2-methylsulfanyl-ethyl)-pyridin-2-yl ester 
• 78428-02-1 4-Phenyl-butyric acid [2,2']bipyridinyl-6-yl ester 
• 78427-98-2 4-Phenyl-butyric acid 6-phenethyl-pyridin-2-yl ester 
• 78428-00-9 4-Phenyl-butyric acid 6-[2-(2-methoxy-ethoxy)-ethyl]-pyridin-2-yl ester 
• 76063-11-1 S-(2-pyridinyl) 4-phenylbutanethioate 
• 1462-75-5 3-phenylpropylmagnesium bromide 
• 638-29-9 n-valeryl chloride 
• 637-59-2 1-Bromo-3-phenylpropane 
• 110-62-3 pentanal 
• 2046-18-6 4-phenylbutyronitrile 

Downstream Products

• 87712-68-3 3-methyl-1-(3-phenylpropyl)cyclopentene 
• 87712-67-2 1-butyl-3-phenylcyclopentene 
• 93184-61-3 oct-3-yn-1-ylbenzene 

Relevant articles and documents

Iminyl Radical-Triggered Intermolecular Distal C(sp3)-H Heteroarylation via 1,5-Hydrogen-Atom Transfer (HAT) Cascade

An efficient iron-catalyzed intermolecular remote C(sp3)-H heteroarylation of alkyl ketones has been developed via an iminyl radical-triggered 1,5-hydrogen-atom transfer (HAT) cascade. This protocol was amenable to a wide variety of alkyl ketones and heteroaryls, thus providing a straightforward method for the late-stage functionalization of alkylketones and heteroaryls.

Experimental and theoretical studies on the reactivities of partially and fully fluorinated primary alkyl radicals

Absolute rate constants for hydrogen abstraction from n-Bu3SnH by a number of partially-fluorinated and fully fluorinated n-alkyl radicals have been measured. The C-H and C-C bond dissociation energies for a number of pertinent hydrofluorocarbons have been calculated by DFT. The rate data are compared with those for addition of the same radicals to styrene, and the reactivities of these radicals are discussed in terms of their electronegativies, their structure and the thermodynamics of their reactions.