58795-27-0

Basic information

• Product Name: (4aS,8aS)-1,1,4a-Trimethyl-5,6-dimethylene-decahydro-naphthalene
• Synonyms: (4aS,8aS)-1,1,4a-Trimethyl-5,6-dimethylene-decahydro-naphthalene
• CAS NO: 58795-27-0
• Molecular Weight: 204.356
• Mol File: 58795-27-0.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (4aS,8aS)-1,1,4a-Trimethyl-5,6-dimethylene-decahydro-naphthalene(CAS DataBase Reference)
• NIST Chemistry Reference: (4aS,8aS)-1,1,4a-Trimethyl-5,6-dimethylene-decahydro-naphthalene(58795-27-0)
• EPA Substance Registry System: (4aS,8aS)-1,1,4a-Trimethyl-5,6-dimethylene-decahydro-naphthalene(58795-27-0)

Safety Data

• Hazardous Substances Data: 58795-27-0(Hazardous Substances Data)

Upstream product

• 596-85-0 manool 

Downstream Products

• 39707-56-7 (+)-zonarone 
• 39707-54-5 (-)-ent-zonarol 
• 478930-78-8 (-)-ent-zonarol di-THP ether 
• 478930-77-7 [2,5-bis-(tetrahydro-pyran-2-yloxy)-phenyl]-(5,5,8a-trimethyl-2-methylene-decahydro-naphthalen-1-yl)-methanol 
• 50490-43-2 euryfuran 
• 15340-78-0 12-acetoxy-15,16-dinor-pymara-8,11,13-triene 
• 561-95-5 nimbiol 
• 573969-74-1 (2,5-Dimethoxy-phenyl)-((4aS,8aS)-2,5,5,8a-tetramethyl-3,4,4a,5,6,7,8,8a-octahydro-naphthalen-1-yl)-methanol 
• 573969-75-2 (4aS,8aS)-8-(2,5-Dimethoxy-benzyl)-4,4,7,8a-tetramethyl-1,2,3,4,4a,5,6,8a-octahydro-naphthalene 
• 573983-71-8 isozonarone Δ^8,9 

Relevant articles and documents

First formal synthesis of (+)-nimbidiol. Synthesis, X-ray structure and anticancer activity of a novel ring C aromatic diterpene: Dimethyl (+)-podocarpa-8,11,13-triene-12,13-dicarboxylate

A novel ring C aromatic diterpene (4) has been prepared in three steps from natural (+)-manool (1). The structure and anticancer activity data for 4 has been investigated. This key intermediate (4) was easily transformed into 7-deoxo nimbidiol dimethyl ether (8). The present work represents the first formal synthesis of (+)-nimbidiol (10).