861996-70-5

Basic information

• Product Name: ((1S,2S,4aS,8aR)-5,5,8a-Trimethyl-1-{2-[1-(toluene-4-sulfonyl)-1H-indol-2-yl]-ethyl}-decahydro-naphthalen-2-yl)-methanol
• Synonyms: ((1S,2S,4aS,8aR)-5,5,8a-Trimethyl-1-{2-[1-(toluene-4-sulfonyl)-1H-indol-2-yl]-ethyl}-decahydro-naphthalen-2-yl)-methanol
• CAS NO: 861996-70-5
• Molecular Weight: 507.737
• Mol File: 861996-70-5.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: ((1S,2S,4aS,8aR)-5,5,8a-Trimethyl-1-{2-[1-(toluene-4-sulfonyl)-1H-indol-2-yl]-ethyl}-decahydro-naphthalen-2-yl)-methanol(CAS DataBase Reference)
• NIST Chemistry Reference: ((1S,2S,4aS,8aR)-5,5,8a-Trimethyl-1-{2-[1-(toluene-4-sulfonyl)-1H-indol-2-yl]-ethyl}-decahydro-naphthalen-2-yl)-methanol(861996-70-5)
• EPA Substance Registry System: ((1S,2S,4aS,8aR)-5,5,8a-Trimethyl-1-{2-[1-(toluene-4-sulfonyl)-1H-indol-2-yl]-ethyl}-decahydro-naphthalen-2-yl)-methanol(861996-70-5)

Safety Data

• Hazardous Substances Data: 861996-70-5(Hazardous Substances Data)

Upstream product

• 3243-36-5 (1S,4aS,8aS)-1,2,3,4,4a,5,6,7,8,8a-decahydro-5,5,8a-trimethyl-2-methylene-1-naphthaleneacetaldehyde 
• 31271-90-6 1-(p-toluenesulfonyl)-1H-indole 
• 861996-62-5 1-[1-(Toluene-4-sulfonyl)-1H-indol-2-yl]-2-((1S,4aS,8aS)-5,5,8a-trimethyl-2-methylene-decahydro-naphthalen-1-yl)-ethanol 
• 861996-66-9 1-(Toluene-4-sulfonyl)-2-[2-((1S,4aS,8aS)-5,5,8a-trimethyl-2-methylene-decahydro-naphthalen-1-yl)-ethyl]-1H-indole 

Downstream Products

• 861996-55-6 (1R,4aS,8aS)-5,5,8a-Trimethyl-1-{2-[1-(toluene-4-sulfonyl)-1H-indol-2-yl]-ethyl}-octahydro-naphthalen-2-one 
• 861996-74-9 (1S,2S,4aS,8aR)-5,5,8a-Trimethyl-1-{2-[1-(toluene-4-sulfonyl)-1H-indol-2-yl]-ethyl}-decahydro-naphthalene-2-carboxylic acid 

Relevant articles and documents

Diversity oriented synthesis of hispanane-like terpene derivatives from (R)-(+)-sclareolide

(R)-(+)-Sclareolide 1 has been used as a starting material to develop a diversity oriented methodology to access hispanane 28 a, and hispanane-like derivatives 27b-27e. This methodology is based on the intramolecular Friedel-Crafts acylation of the corres