86546-84-1

Basic information

• Product Name: (5S,8R,10S)-drim-9⁽¹¹⁾-en-8-ol
• Synonyms: (5S,8R,10S)-drim-9⁽¹¹⁾-en-8-ol
• CAS NO: 86546-84-1
• Molecular Weight: 222.371
• Mol File: 86546-84-1.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: (5S,8R,10S)-drim-9⁽¹¹⁾-en-8-ol(CAS DataBase Reference)
• NIST Chemistry Reference: (5S,8R,10S)-drim-9⁽¹¹⁾-en-8-ol(86546-84-1)
• EPA Substance Registry System: (5S,8R,10S)-drim-9⁽¹¹⁾-en-8-ol(86546-84-1)

Safety Data

• Hazardous Substances Data: 86546-84-1(Hazardous Substances Data)

Upstream product

• 31207-65-5 8α-acetoxy-13,14,15,16-tetranor-12-labdanoic acid 
• 623-00-7 4-bromobenzenecarbonitrile 
• 402-43-7 p-trifluoromethylphenyl bromide 
• 352-34-1 4-fluoro-1-iodobenzene 
• 460-00-4 1-Bromo-4-fluorobenzene 
• 106-39-8 bromochlorobenzene 
• 348-52-7 1-Fluoro-2-iodobenzene 
• 1072-85-1 o-fluorobromobenzene 
• 80098-20-0 8α-(acetyloxy)-14,15-dinorlabdan-13-one 

Downstream Products

• 851279-17-9 19,20-di-O-benzyl-puupehenol-6-ene 
• 468-68-8 (-)-drimenol 
• 851279-15-7 3,4-di-benzyloxy-6-(7'-drimen-11'-ylidene)-2,4-cyclohexadienone 
• 257288-33-8 8-epi-19,20-di-O-benzyl-puupehenol 
• 20404-65-3 (-)-(2R,4aS,8aS)-2,5,5,8a-Tetramethyl-3,4,4a,5,6,7,8,8a-octahydronaphthalen-1(2H)-one 
• 39707-54-5 (-)-ent-zonarol 
• 250146-75-9 ent-isozonarol 
• 39707-56-7 (+)-zonarone 
• 39707-59-0 ent-isozonarone 
• 752211-90-8 4-hydroxy-3-(((1R,2R,4aS,8aS)-2-hydroxy-2,5,5,8a-tetramethyldecahydronaphthalen-1-yl)methyl)benzoic acid 
• 1376654-81-7 C₃₆H₄₄O₄ 
• 1376654-71-5 C₂₃H₃₄O₃ 
• 1376654-68-0 (1R,2R,4aS,8aS)-2,5,5,8a-tetramethyl-1-(4-(trifluoromethyl)benzyl) decahydronaphthalen-2-ol 
• 1376654-34-0 (+)-yahazunone 

Relevant articles and documents

Modular Synthesis of Drimane Meroterpenoids Leveraging Decarboxylative Borylation and Suzuki Coupling

Drimane meroterpenoids have attracted an increasing amount of attention in the discovery of therapeutically important probes, while the laggard synthetic accessibility is a conspicuous challenge. A new paradigm merging decarboxylative borylation and Suzuki coupling was developed as a powerful platform. Key features include the mild conditions, good chemoselectivity, operational facility, scalability, and easy availability of the coupling partners. This practical strategy enables the expedient formal synthesis of a large number of natural products and rapid generation of analogues.