4380-91-0

Basic information

• Product Name: Hexanoic acid, 3-oxo-
• CAS NO: 4380-91-0
• Molecular Formula: C6H10O3
• Molecular Weight: 130.144
• Mol File: 4380-91-0.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: Hexanoic acid, 3-oxo-(CAS DataBase Reference)
• NIST Chemistry Reference: Hexanoic acid, 3-oxo-(4380-91-0)
• EPA Substance Registry System: Hexanoic acid, 3-oxo-(4380-91-0)

Safety Data

• Hazardous Substances Data: 4380-91-0(Hazardous Substances Data)

Upstream product

• 142-62-1 hexanoic acid 

Downstream Products

• 3249-68-1 ethyl butyroyl acetate 
• 91298-66-7 (S)-2-aminopentanonic acid 
• 18742-93-3 3-butyryl-4-hydroxy-6-propyl-2H-pyran-2-one 
• 80359-93-9 3-phenyl-1-octen-5-one 
• 1533453-10-9 6-cyclohexyloct-7-en-4-one 
• 1533453-26-7 6-benzyl-6-methyloct-7-en-4-one 
• 1447666-79-6 4-methyl-N-(3-oxo-1-phenylhexyl)benzenesulfonamide 
• 1403814-86-7 (R)-4-methoxy-N-(3-oxo-1-phenylhexyl)benzenesulfonamide 
• 4909-19-7 1,1-di(p-tolyl)pentan-3-one 
• 912837-94-6 1-(4-nitrophenyl)-5-n-propyl-1H-1,2,3-triazole-4-carboxylic acid 
• 1159275-99-6 [5-(3-oxohexanoylamino)-1-phenylcarbamoylpentyl]carbamic acid benzyl ester 
• 30414-54-1 methyl 3-oxohexanoate 

Relevant articles and documents

On the Oxygenation of Several Aromatic and Aliphatic Compounds with Aqueous Ferrous Ion-molecular Oxygen

Hydroxylation was shown to occur readily in the reactions of aromatic compounds siuch as benzoic acid, nitrobenzene, acetanilide, and phenol with ferrous ion-molecular oxygen in 0.5M phosphate buffer (pH 6.8) at 40 deg C for 3 h.The yields of hydroxylated products were higher than those obtained with other reported hydroxylation systems of transition metal-molecular oxygen.The NIH shift was not observed in the title reactions of C(4)-deuterioacetanilide and C(4)-deuteriobenzoic acid.This system was also demonstrated to oxygenate caproic acid to give a mixture of 3-, 4-, and 5-oxocaproic acids in 67percent total yield. Keywords ---- hydroxylation of aromatic compound; ferrous ion; molecular oxygen; benzoic acid; nitrobenzene; acetanilide; phenol; NIH shift; oxygenation of caproic acid; GC-MS of methyl oxocaproate