6584-69-6

Basic information

• Product Name: Acetic acid (3S,3aR,5aS,9S,11aS)-3-((S)-5,5-dimethyl-tetrahydro-furan-2-yl)-3a-hydroxy-3,5a,8,8,11a-pentamethyl-1-oxo-3a,4,5,5a,7,7a,8,9,10,11,11a,13-dodecahydro-3H-2-oxa-pentaleno[1,6a-a]phenanthren-9-yl ester
• CAS NO: 6584-69-6
• Molecular Weight: 526.714
• Mol File: 6584-69-6.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: Acetic acid (3S,3aR,5aS,9S,11aS)-3-((S)-5,5-dimethyl-tetrahydro-furan-2-yl)-3a-hydroxy-3,5a,8,8,11a-pentamethyl-1-oxo-3a,4,5,5a,7,7a,8,9,10,11,11a,13-dodecahydro-3H-2-oxa-pentaleno[1,6a-a]phenanthren-9-yl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Acetic acid (3S,3aR,5aS,9S,11aS)-3-((S)-5,5-dimethyl-tetrahydro-furan-2-yl)-3a-hydroxy-3,5a,8,8,11a-pentamethyl-1-oxo-3a,4,5,5a,7,7a,8,9,10,11,11a,13-dodecahydro-3H-2-oxa-pentaleno[1,6a-a]phenanthren-9-yl ester(6584-69-6)
• EPA Substance Registry System: Acetic acid (3S,3aR,5aS,9S,11aS)-3-((S)-5,5-dimethyl-tetrahydro-furan-2-yl)-3a-hydroxy-3,5a,8,8,11a-pentamethyl-1-oxo-3a,4,5,5a,7,7a,8,9,10,11,11a,13-dodecahydro-3H-2-oxa-pentaleno[1,6a-a]phenanthren-9-yl ester(6584-69-6)

Safety Data

• Hazardous Substances Data: 6584-69-6(Hazardous Substances Data)

Upstream product

• 11052-32-7 holothurin B 
• 108-24-7 acetic anhydride 
• 6853-99-2 22,25-oxidoholothurinogenin 
• 67304-16-9 3-O-(2'-β-D-quinovopyranosyl-β-D-xylopyranosyl)holothurinogenol 
• 112595-64-9 3-O-(β-D-xylopyranosyl)-22,25-oxidoholothurinogenin 
• 94750-76-2 3β,12α-diacetoxy-7,8-dihydro-22,25-oxidoholothurinogenin 
• 23199-71-5 3β-acetoxy-12β-methoxy-22,25-oxido-7,8-dihydroholothurinogenin 
• 6853-99-2 22,25-epoxyholosta-7,9(11)-diene-3β,17α-diol 

Relevant articles and documents

Triterpene Glycosides and Aglycones of Sea Cucumbers Holothuria atra and H. scabra (Holothurideae)

From the acid hydrolysates of the methanol extracts of the sea cucumbers Holothuria atra and H. scabra (phylum: echinodermata; fam: Holothurideae) collected at Mandapam coast (Tamil Nadu), a total of nine Holothuria sapogenins (compounds A-G, L and M) and two glycosides (H and K) have been isolated by column chromatography and characterised by spectral (UV, IR, PMR and mass) data.Compound C is established as the novel 11-keto-9(11)-dihydro-22,25-oxidoholothurinogenin (III).Compound D (isolated as acetate) is the new 3β-acetoxy-12β-methoxy-7,8-dihydroholothurinogenin (IVa).Compounds F and G (isolated as acetates) are identified as 3β,12α-diacetoxy-7,8-dihydroholothurinogenin (VIa) and 3β,12α-diacetoxy-7,8-dihydro-22,25-oxidoholothurinogenin (VIIa) respectively.For the first time, these two genuine aglycones have been isolated as survivors of acid hydrolysis.Glycoside H is identified as the unique 3-O-(β-D-xylopyranosyl)-22,25-oxidoholothurinogenin (VIII).The remaining six compounds (A, B, E, L, M and glycoside K) are all known compounds; however these are reported for the first time from H. atra and H. scabra (except compound A in both and compound B in H. atra).