929803-84-9

Basic information

• Product Name: N-[2-benzenesulfonyl-6-(tert-butyl-dimethyl-silanyloxy)-8a-formyl-1,2,3,4,4a,5,8,8a-octahydro-isoquinolin-8-yl]-2-chloro-acetamide
• Synonyms: N-[2-benzenesulfonyl-6-(tert-butyl-dimethyl-silanyloxy)-8a-formyl-1,2,3,4,4a,5,8,8a-octahydro-isoquinolin-8-yl]-2-chloro-acetamide
• CAS NO: 929803-84-9
• Molecular Weight: 527.157
• Mol File: 929803-84-9.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: N-[2-benzenesulfonyl-6-(tert-butyl-dimethyl-silanyloxy)-8a-formyl-1,2,3,4,4a,5,8,8a-octahydro-isoquinolin-8-yl]-2-chloro-acetamide(CAS DataBase Reference)
• NIST Chemistry Reference: N-[2-benzenesulfonyl-6-(tert-butyl-dimethyl-silanyloxy)-8a-formyl-1,2,3,4,4a,5,8,8a-octahydro-isoquinolin-8-yl]-2-chloro-acetamide(929803-84-9)
• EPA Substance Registry System: N-[2-benzenesulfonyl-6-(tert-butyl-dimethyl-silanyloxy)-8a-formyl-1,2,3,4,4a,5,8,8a-octahydro-isoquinolin-8-yl]-2-chloro-acetamide(929803-84-9)

Safety Data

• Hazardous Substances Data: 929803-84-9(Hazardous Substances Data)

Upstream product

• 929803-76-9 1-benzenesulfonyl-1,2,5,6-tetrahydropyridine-3-carboxaldehyde 
• 929803-83-8 (4aS,8S,8aS)-N-allyl-N-[2-benzenesulfonyl-6-(tert-butyldimethylsiloxy)-8a-formyl-1,2,3,4,4a,5,8,8a-octahydroisoquinolin-8-yl]chloroacetamide 
• 98-09-9 benzenesulfonyl chloride 
• 300-08-3 arecoline hydrobromide 
• 69739-34-0 t-butyldimethylsiyl triflate 
• 929803-77-0 N-allyl-N-[(E)-3-(tert-butyldimethylsiloxy)-1,3-butadienyl]chloroacetamide 
• 929803-75-8 methyl 1-benzenesulfonyl-1,2,5,6-tetrahydropyridine-3-carboxylate 

Downstream Products

• 929803-85-0 3-[2-benzenesulfonyl-6-(tert-butyl-dimethyl-silanyloxy)-8-(2-chloro-acetylamino)-2,3,4,4a,5,8-hexahydro-1H-isoquinolin-8a-yl]-acrylic acid ethyl ester 
• 929803-87-2 C₂₄H₃₁ClN₂O₇S 

Relevant articles and documents

Synthetic study of manzamine B: synthesis of the tricyclic central core by an asymmetric Diels-Alder and RCM strategy

Tricyclic core of manzamine B was successfully synthesized through asymmetric Diels-Alder reaction and RCM strategy. Cr-salen-F complex was found to be the most effective catalyst in DA reaction of aminodienes with heterocyclic dienophiles to give up to 9