38284-28-5

Basic information

• Product Name: nonane-2,5,8-trione
• Synonyms: 2,5,8-Nonanetrione
• CAS NO: 38284-28-5
• Molecular Formula: C₉H₁₄O₃
• Molecular Weight: 170.2057
• Mol File: 38284-28-5.mol
• Article Data: 13

Chemical Properties

• Boiling Point: 305.8°C at 760 mmHg
• Flash Point: 128.1°C
• Density: 1.01g/cm³
• Vapor Pressure: 0.000804mmHg at 25°C
• Refractive Index: 1.433
• CAS DataBase Reference: nonane-2,5,8-trione(CAS DataBase Reference)
• NIST Chemistry Reference: nonane-2,5,8-trione(38284-28-5)
• EPA Substance Registry System: nonane-2,5,8-trione(38284-28-5)

Safety Data

• Hazardous Substances Data: 38284-28-5(Hazardous Substances Data)

Upstream product

• 13679-56-6 4-(5-methyl-furan-2-yl)-butan-2-one 
• 1890-28-4 divinylketone 
• 75-07-0 acetaldehyde 
• 50-00-0 formaldehyd 
• 78-94-4 methyl vinyl ketone 
• 75-52-5 nitromethane 
• 626-96-0 4-oxopentanal 
• 7647-01-0 hydrogenchloride 
• 1071-73-4 5-Hydroxy-2-pentanone 
• 534-22-5 2-methylfuran 
• 620-02-0 5-Methylfurfural 
• 66434-99-9 (E)-4-(5-Methyl-furan-2-yl)-but-3-en-2-one 
• 888014-45-7 3-(hydroxymethyl)-2-furaldehyde 
• 1245713-17-0 4-(5-hydroxy methyl)-2-furanyl-2-butanone 

Downstream Products

• 1179428-54-6 2-[2-(1,3-dimethyl-2-[2-(1,2,3-trimethyl-2,3-dihydro-1H-2-perimidinyl)ethyl]-2,3-dihydro-1H-2-perimidinyl)ethyl]-1,2,3-trimethyl-2,3-dihydro-1H-perimidine 
• 111-84-2 nonane 

Relevant articles and documents

Synthesis of Two 2-(Oxoalkyl)-3-methyl-2-cyclopentenones

Reported here are the preparations of 2-(2-oxopropyl)-3-methyl-2-cyclopentenone and the 2,2-dimethyl-1,3-propanediol ketal of 2-(3-oxobutyl)-3-methyl-2-cyclopentenone.A reagent for the convenient preparation of such cyclic ketals is described.

A diesel oil or aviation kerosene cyclanes for process for the preparation of (by machine translation)

The invention is in the field of organic synthesis, relates to a diesel oil or aviation kerosene cyclanes for the preparation method. Method is as follows: 1) lignocellulolytic yl furan compound and carbonyl compound is subjected to acid or alkali catalys

Hydrogenation/hydrolytic ring opening of 5-HMF by Cp-Iridium(III) half-sandwich complexes for bioketones synthesis

A new method for one-step synthesis of ketones from biobased 5-hydroxymethylfurfural (5-HMF) and its derivatives is reported. Bipyridine coordinated Cp-Iridium(III) complexes (Cp, 1,2,3,4,5-pentamethylcyclopenta-1,3-diene) exhibit highly efficient catalytic performance for hydrogenation/hydrolytic ring opening of 5-HMF and derivatives to produce ketones. The catalytic mechanism is proposed to proceed via carbonyl hydrogenation, hydroxyl group promoted and directed hydrolytic furan ring opening, followed by hydrogenation of α,β-unsaturated carbonyl compound based on the experimental and independent events' statistical calculation results. (Chemical Equation Presented).