956964-09-3

Basic information

• Product Name: C₉H₁₄O₄C₈H₈O
• Synonyms: C₉H₁₄O₄C₈H₈O
• CAS NO: 956964-09-3
• Molecular Weight: 306.359
• Mol File: 956964-09-3.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: C₉H₁₄O₄C₈H₈O(CAS DataBase Reference)
• NIST Chemistry Reference: C₉H₁₄O₄C₈H₈O(956964-09-3)
• EPA Substance Registry System: C₉H₁₄O₄C₈H₈O(956964-09-3)

Safety Data

• Hazardous Substances Data: 956964-09-3(Hazardous Substances Data)

Upstream product

• 595581-64-9 (3aR,6aR)-2,2-dimethyltetrahydro-4H-cyclopenta[d][1,3]dioxol-4-one 
• 683276-43-9 (4R,5R)-1-(2,2-dimethyl-5-vinyl-[1,3]dioxolan-4-yl)prop-2-en-1-ol 
• 160701-58-6 tert-butyldimethylsilyl 3-(2-hydroxyethyl)phenyl ether 
• 115509-13-2 (3aR,6aR)-2,2-Dimethyl-3a,6a-dihydro-cyclopenta[1,3]dioxol-4-one 
• 951377-89-2 [(3aS,4E,5S,6aR)-4-ethylidene-2,2-dimethyltetrahydro-3aH-cyclopenta[d][1,3]dioxol-5-yl]acetic acid 2-[3-(tert-butyldimethylsilyloxy)phenyl]ethyl ester 
• 869476-95-9 [(3aS,4E,5S,6aR)-4-ethylidene-2,2-dimethyltetrahydro-3aH-cyclopenta[d][1,3]dioxol-5-yl]acetic acid 
• 869476-94-8 [(3aS,4E,5S,6aR)-4-ethylidene-2,2-dimethyltetrahydro-3aH-cyclopenta[d][1,3]dioxol-5-yl]acetic acid methyl ester 
• 869476-93-7 ((3aR,5S,6aR)-2,2-dimethyl-4-oxotetrahydro-3aH-cyclopenta[d][1,3]dioxol-5-yl)acetic acid methyl ester 

Relevant articles and documents

Syntheses of (-)-oleocanthal, a natural NSAID found in extra virgin olive oil, the (-)-deacetoxy-oleuropein aglycone, and related analogues

(Chemical Equation Presented) Phenolic compounds extracted from extra virgin olive oil have attracted considerable recent attention. One of the components, (-)-oleocanthal (1), an inhibitor of the COX-1 and COX-2 enzymes, possesses similar potency as the NSAID ibuprofen. In this, a full account, we disclose the first- and now second-generation syntheses of both enantiomers of the oleocanthals, as well as the first synthesis of the closely related (-)-deacetoxy-oleuropein aglycone and a series of related analogues for structure activity studies. To demonstrate the utility of the second-generation synthesis, multigram quantities of (-)-oleocanthal were prepared in 10 steps (14% overall yield) from commercially available D-lyxose.