63434-46-8

Basic information

• Product Name: 4-Heptanone, 1,7-diphenyl-
• CAS NO: 63434-46-8
• Molecular Formula: C19H22O
• Molecular Weight: 266.383
• Mol File: 63434-46-8.mol
• Article Data: 9

Chemical Properties

• CAS DataBase Reference: 4-Heptanone, 1,7-diphenyl-(CAS DataBase Reference)
• NIST Chemistry Reference: 4-Heptanone, 1,7-diphenyl-(63434-46-8)
• EPA Substance Registry System: 4-Heptanone, 1,7-diphenyl-(63434-46-8)

Safety Data

• Hazardous Substances Data: 63434-46-8(Hazardous Substances Data)

Upstream product

• 868-84-8 S,S-dimethyl dithiocarbonate 
• 637-59-2 1-Bromo-3-phenylpropane 
• 1462-75-5 3-phenylpropylmagnesium bromide 
• 177756-65-9 N-methoxy-N-methyl-4-phenylbutyramide 
• 3155-16-6 diphenyl oxalate 
• 4119-41-9 1-iodo-3-phenylpropan 
• 3742-75-4 3-phenylpropyl 4-methylbenzenesulfonate 
• 541-41-3 chloroformic acid ethyl ester 
• 26272-90-2 cetyl chloroformate 

Downstream Products

• 124319-52-4 trans-2(S)-<(tert-butoxycarbonyl)amino>-1,8-diphenyl-5-(3-phenylpropyl)-3-octene 
• 199990-05-1 4-(5-Ethyl-1-methyl-4-{3-[5-phenyl-2-(3-phenyl-propyl)-pentylamino]-benzoyl}-1H-pyrrol-2-yl)-butyric acid ethyl ester 
• 344462-29-9 5-Phenyl-2-(3-phenyl-propyl)-pentan-1-ol 
• 344462-33-5 C₂₀H₂₅Br 
• 124319-51-3 5-phenyl-2-(3-phenylpropyl)pentan-1-al 
• 878142-71-3 3-fluoro-1,7-diphenyl-heptan-4-one 

Relevant articles and documents

Radical carbonylation with [11C]carbon monoxide promoted by oxygen-centered radicals: Experimental and DFT studies of the mechanism

Photoinitiated carbonylation of alkyl iodides with [11C]carbon monoxide (11C t1/2 = 20.4 min) is enhanced by ketones that have lowest-lying excited triplet state of nπ* character. For example, adding 5 mol % of acetophenon

From Alkyl Halides to Ketones: Nickel-Catalyzed Reductive Carbonylation Utilizing Ethyl Chloroformate as the Carbonyl Source

Ketones are an important class of molecules in synthetic and medicinal chemistry. Rapid and modular synthesis of ketones remains in high demand. Described here is a nickel-catalyzed three-component reductive carbonylation method for the synthesis of dialkyl ketones. A wide range of both symmetric and asymmetric dialkyl ketones can be accessed from alkyl halides and a safe CO source, ethyl chloroformate. The approach offers complementary substrate scope to existing carbonylation methods while avoiding the use of either toxic CO or metal carbonyl reagents.

RETROVIRAL PROTEASE INHIBITING COMPOUNDS

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