109296-10-8

Basic information

• Product Name: 2-Nonen-4-ol, 1,1-dimethoxy-, (2E)-
• CAS NO: 109296-10-8
• Molecular Formula: C11H22O3
• Molecular Weight: 202.294
• Mol File: 109296-10-8.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 2-Nonen-4-ol, 1,1-dimethoxy-, (2E)-(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Nonen-4-ol, 1,1-dimethoxy-, (2E)-(109296-10-8)
• EPA Substance Registry System: 2-Nonen-4-ol, 1,1-dimethoxy-, (2E)-(109296-10-8)

Safety Data

• Hazardous Substances Data: 109296-10-8(Hazardous Substances Data)

Upstream product

• 67-56-1 methanol 
• 791615-15-1 1-(4-hydroxy-2-nonenyloxy)-2-propyl-9,10-anthraquinone 

Downstream Products

• 119008-08-1 (-) 4-hydroxy-2-nonenal 
• 850480-50-1 4-hydroxynon-2-enal 
• 128860-97-9 (5Z,8Z,10E)-(S)-12-(tert-Butyl-diphenyl-silanyloxy)-heptadeca-5,8,10-trienoic acid methyl ester 
• 128860-96-8 (5Z,8Z,10E)-(R)-12-(tert-Butyl-diphenyl-silanyloxy)-heptadeca-5,8,10-trienoic acid methyl ester 
• 128860-98-0 Benzoic acid (2E,4Z,7Z)-(S)-11-methoxycarbonyl-1-pentyl-undeca-2,4,7-trienyl ester 
• 128860-93-5 tert-Butyl-[(S)-1-((E)-3,3-dimethoxy-propenyl)-hexyloxy]-diphenyl-silane 
• 128860-92-4 tert-Butyl-[(R)-1-((E)-3,3-dimethoxy-propenyl)-hexyloxy]-diphenyl-silane 
• 128946-66-7 (E)-(S)-1-((4S,5S)-1,3-Dimethyl-4,5-diphenyl-imidazolidin-2-yl)-oct-1-en-3-ol 
• 128860-91-3 (E)-(R)-1-((4S,5S)-1,3-Dimethyl-4,5-diphenyl-imidazolidin-2-yl)-oct-1-en-3-ol 
• 128860-94-6 methyl 13(S)-(tert-butyldiphenylsilyloxy)octadeca-9(Z),11(E)-dienoate 
• 118908-11-5 ether silyle du coriolate de methyle 
• 128860-95-7 ether silyle du tetranorcoriolate de methyle 
• 118908-12-6 ether silyle du coriolate de methyle 
• 118908-10-4 (E)-(R)-4-(tert-Butyl-diphenyl-silanyloxy)-non-2-enal 

Relevant articles and documents

Caged trans-4-hydroxy-2-nonenal

(Chemical Equation Presented) A caged 4-hydroxy-2-nonenal (4-HNE) has been prepared and its photochemistry investigated. Upon photolysis, 1 releases 4-HNE in up to 100% yield. From these photolyses, 4-HNE could be isolated in up to 91% yield. 4-HNE is produced under either aerobic or anaerobic conditions. The caging strategy does not require prior preparation of 4-HNE and, therefore, represents a three-step synthetic route to the bioactive enal in 48% overall yield.