134071-04-8

Basic information

• Product Name: 2-myristoylcyclohexane-1,3-dione
• Synonyms: 2-myristoylcyclohexane-1,3-dione
• CAS NO: 134071-04-8
• Molecular Weight: 322.488
• Mol File: 134071-04-8.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 2-myristoylcyclohexane-1,3-dione(CAS DataBase Reference)
• NIST Chemistry Reference: 2-myristoylcyclohexane-1,3-dione(134071-04-8)
• EPA Substance Registry System: 2-myristoylcyclohexane-1,3-dione(134071-04-8)

Safety Data

• Hazardous Substances Data: 134071-04-8(Hazardous Substances Data)

Upstream product

• 504-02-9 1,3-cylohexanedione 
• 626-29-9 myristic anhydride 
• 125651-15-2 Tetradecanoic acid 3-oxo-cyclohex-1-enyl ester 
• 112-64-1 tetradecanoyl chloride 

Downstream Products

• 113201-68-6 1-(2',6'-dihydroxyphenyl)tetradecan-1-one 

Relevant articles and documents

ANTIBACTERIAL AGENTS AGAINST DRUG-RESISTANT STAPHYLOCOCCUS AUREUS OR VANCOMYCIN-RESISTANT ENTEROCOCCUS AND ANTIFUNGAL AGENTS COMPRISING STEPHANITIS SVENSONI-DERIVED POLYKETIDE OR SYNTHETIC ANALOGS THEREOF

PROBLEM TO BE SOLVED: To provide antibacterial or antifungal agents comprising a naturally occurring substance or synthetic analogs thereof having high antibacterial activity against methicillin-resistant Staphylococcus aureus or vancomycin-resistant Ente

New 2-Acylcyclohexane-1,3-diones: Kairomone Components against a Parasitic Wasp, Venturia canescens, from Feces of the Almond Moth, Cadra cautella, and the Indian Meal Moth. Plodia interpunctella

As new kairomone components, 2-palmitoyl- (I) and 2-stearoylcyclohexane-1,3-dione (II) were identified for the parasitic wasp Venturia canescens from feces of the Indian meal moth larva, Plodia interpunctella.One more component, 2-arachidoylcyclohexane-1,3-dione (III), together with the afore mentioned two compounds were newly obtained from feces of the almond moth larva Cadra cautella. I 2-Palmitoylcyclohexane-1,3-dione II 2-Stearoylcyclohexane-1,3-dione III 2-Arachidoylcyclohexane-1,3-dione.Purified kairomone fractions from both species indicated similar activity to synthetic 2-oleoylcyclohexane-1,3-dione (active at 0.1 mg/ml). 2-Palmitoylcyclohexane-1,3-dione (I) was the most active (at 1 mg/ml) among the synthetic homologues with saturated 2-acyl groups.No traces of 2-acylcyclohexane-1,3-dione were found in the rearing medium of the host; therefore, the kairomone was suggested to have been biosynthesized.