40898-19-9

Basic information

• Product Name: 2,3-Pentanedione, 4,4-dimethyl-
• Synonyms: 4,4-Dimethyl-pentan-2,3-dion;2,3-Pentanedione,4,4-dimethyl;4,4-dimethyl-pentane-2,3-dione;4,4-dimethyl-2,3-pentanedione
• CAS NO: 40898-19-9
• Molecular Formula: C7H12O2
• Molecular Weight: 128.171
• Mol File: 40898-19-9.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 2,3-Pentanedione, 4,4-dimethyl-(CAS DataBase Reference)
• NIST Chemistry Reference: 2,3-Pentanedione, 4,4-dimethyl-(40898-19-9)
• EPA Substance Registry System: 2,3-Pentanedione, 4,4-dimethyl-(40898-19-9)

Safety Data

• Hazardous Substances Data: 40898-19-9(Hazardous Substances Data)

Upstream product

• 67-56-1 methanol 
• 999-78-0 4,4-dimethyl-2-pentyne 
• 105440-03-7 N-(5-methyl-2-oxo-1,3-dioxol-4-yl)methyl NFLX (5-methyl-2-oxo-1,3-dioxol-4-yl)methyl ester 
• 86761-10-6 N-(5-tert-butyl-2-oxo-1,3-dioxol-4-yl)methyl NFLX 

Downstream Products

• 100883-45-2 5,5-dimethyl-1t-phenyl-hex-1-ene-3,4-dione 
• 87898-97-3 N,N-Dibenzyl-4,4-dimethyl-2,3-dioxopentanthioamid 

Relevant articles and documents

Oxidation of Alkynes by Hydrogen Peroxide Catalyzed by Methylrhenium Trioxide

The oxidation of alkynes with hydrogen peroxide is catalyzed by methylrhenium tioxide.The reactions can be rationalized by postulating that an oxirene intermediate is formed between a rhenium peroxide and the alkyne.Internal alkynes yield α-diketones and carboxylic acids, the latter from the complete cleavage of the triple bonds.Rearrangement products were observed only for aliphatic alkynes.Terminal alkynes gave carboxylic acids and their derivatives and α-keto acids as the major products, but their yields varied with the solvent used.

Studies on prodrugs. IV. Preparation and characterization of N-(5-substituted 2-oxo-1,3-dioxol-4-yl)methyl norfloxacin

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