916085-36-4

Basic information

• Product Name: Benzenesulfonamide, 4-methyl-N-[1-(2-propen-1-yl)-2-[6-[2-[[tris(1-methylethyl)silyl]oxy]ethyl]-1 ,3-benzodioxol-5-yl]-2-cyclopenten-1-yl]-
• CAS NO: 916085-36-4
• Molecular Formula: C33H47NO5SSi
• Molecular Weight: 597.891
• Mol File: 916085-36-4.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: Benzenesulfonamide, 4-methyl-N-[1-(2-propen-1-yl)-2-[6-[2-[[tris(1-methylethyl)silyl]oxy]ethyl]-1 ,3-benzodioxol-5-yl]-2-cyclopenten-1-yl]-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzenesulfonamide, 4-methyl-N-[1-(2-propen-1-yl)-2-[6-[2-[[tris(1-methylethyl)silyl]oxy]ethyl]-1 ,3-benzodioxol-5-yl]-2-cyclopenten-1-yl]-(916085-36-4)
• EPA Substance Registry System: Benzenesulfonamide, 4-methyl-N-[1-(2-propen-1-yl)-2-[6-[2-[[tris(1-methylethyl)silyl]oxy]ethyl]-1 ,3-benzodioxol-5-yl]-2-cyclopenten-1-yl]-(916085-36-4)

Safety Data

• Hazardous Substances Data: 916085-36-4(Hazardous Substances Data)

Upstream product

• 119054-94-3 2-(2'-bromo-4',5'-methylenedioxyphenyl)ethanol 
• 62685-53-4 3-allyl-2-cyclopenten-1-one 
• 73057-68-8 rac-1-allylcyclopent-2-enol 
• 6006-82-2 3,4-methylenedioxyphenethyl alcohol 
• 42185-92-2 3-allylcyclopent-2-en-1-ol 
• 930-30-3 cyclopent-2-enone 
• 916085-32-0 [2-(6-bromo-1,3-benzodioxol-5-yl)ethoxy]-triisopropyl-silane 

Downstream Products

• 916085-39-7 3-[4-[(4-methylphenyl)sulfonyl]-2,4,5,6-tetrahydrocyclopenta[a][1,3]dioxolo[4,5-h][3]benzazepin-3(3H)-yl]-1-propanol 
• 916085-38-6 3a-allyl-4-[(4-methylphenyl)sulfonyl]-2,3,3a,4,5,6-hexahydrocyclopenta[a][1,3]dioxolo[4,5-h][3]benzazepine 
• 916085-37-5 N-{1-allyl-2-[6-(2-hydroxy-ethyl)-1,3-benzodioxol-5-yl]-2-cyclopenten-1-yl}-4-methylbenzenesulfonamide 

Relevant articles and documents

New route to azaspirocycles via the organolithium-mediated conversion of β-alkoxy aziridines into cyclopentenyl amines

(Chemical Equation Presented) A new three-step route to azaspirocycles involving the organolithium-mediated conversion of β-alkoxy aziridines into substituted cyclopentenyl amines, hydroboration, and cyclization has been developed. The methodology is util