117416-34-9

Basic information

• Product Name: N-<<1,2,3,3a,4,5,6,8a-octahydro-7-(1-methylethenyl)-3a-trans-azulenyl>carbonyl>-p-toluenesulfonamide
• CAS NO: 117416-34-9
• Molecular Weight: 373.516
• Mol File: 117416-34-9.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: N-<<1,2,3,3a,4,5,6,8a-octahydro-7-(1-methylethenyl)-3a-trans-azulenyl>carbonyl>-p-toluenesulfonamide(CAS DataBase Reference)
• NIST Chemistry Reference: N-<<1,2,3,3a,4,5,6,8a-octahydro-7-(1-methylethenyl)-3a-trans-azulenyl>carbonyl>-p-toluenesulfonamide(117416-34-9)
• EPA Substance Registry System: N-<<1,2,3,3a,4,5,6,8a-octahydro-7-(1-methylethenyl)-3a-trans-azulenyl>carbonyl>-p-toluenesulfonamide(117416-34-9)

Safety Data

• Hazardous Substances Data: 117416-34-9(Hazardous Substances Data)

Upstream product

• 97997-94-9 Methanesulfonic acid 6-trimethylsilanyl-hex-4-ynyl ester 
• 76711-41-6 1-(Trimethylsilyl)-2-hexyn-6-ol 
• 88996-02-5 6-iodo-1-(trimethylsilyl)-2-hexyne 
• 117416-10-1 (3R,3aS,6aR)-3-Ethoxy-hexahydro-cyclopenta[c]pyrrol-1-one 
• 62506-05-2 cyclopentane-1,2-dicarboximide 
• 15681-48-8 lithium dimethylcuprate 
• 117416-31-6 (1R,5R,6R)-12-(Toluene-4-sulfonyl)-7-vinylidene-12-aza-tricyclo[4.4.2.0^1,5]dodecan-11-one 
• 117416-21-4 rel-(2aR,5aR,6S)-1-(tert-butyldimethylsilyl)-6-ethoxy-2a,3,4,5,5a,6-hexahydro-6a-<6-(trimethylsilyl)-4-hexynyl>-2H-cyclopentapyrrol-2-one 
• 117416-27-0 rel-(1R,2R)-11-(tert-butyldimethylsilyl)-10-vinylidene-11-azatricyclo<4.4.2.0^2,6>dodecan-12-one 
• 117416-12-3 rel-(2aR,5aS,6R)-1-(tert-butyldimethylsilyl)-6-ethoxy-2a,3,4,5,5a,6-hexahydro-2H-cyclopenta-pyrrol-2-one 
• 117416-28-1 rel-(1R,2R)-10-vinylidene-11-azatricyclo<4.4.2.0^2,6>dodecan-12-one 

Relevant articles and documents

INTRAMOLECULAR REACTIONS OF-PROPYNYLSILANES WITH N-ACYLIMINIUM; CUPRATES SN2' REACTIONS OF THE ALLENIC PRODUCTS AS A ROUTE TO TRANS-FUSED CARBOBICYCLES

Intramolecular acid-assisted reactions of 2-propynylsilanes with cyclic N-acyliminium ion precursors lead to bridged azabicyclic systems 34-45 (Table I), containing the uncommon α-allenic amide funcionality.After introduction of a tert-butoxycarbonyl or a