1529806-92-5

Basic information

• Product Name: 9-benzyl-7-chloro-4'-methyl-1',2-ditosyl-1,1',2,3,5',9-hexa-hydrospiro[pyrido[3,4-b]indole-4,2'-pyrrole]
• Synonyms: 9-benzyl-7-chloro-4'-methyl-1',2-ditosyl-1,1',2,3,5',9-hexa-hydrospiro[pyrido[3,4-b]indole-4,2'-pyrrole]
• CAS NO: 1529806-92-5
• Molecular Weight: 672.269
• Mol File: 1529806-92-5.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 9-benzyl-7-chloro-4'-methyl-1',2-ditosyl-1,1',2,3,5',9-hexa-hydrospiro[pyrido[3,4-b]indole-4,2'-pyrrole](CAS DataBase Reference)
• NIST Chemistry Reference: 9-benzyl-7-chloro-4'-methyl-1',2-ditosyl-1,1',2,3,5',9-hexa-hydrospiro[pyrido[3,4-b]indole-4,2'-pyrrole](1529806-92-5)
• EPA Substance Registry System: 9-benzyl-7-chloro-4'-methyl-1',2-ditosyl-1,1',2,3,5',9-hexa-hydrospiro[pyrido[3,4-b]indole-4,2'-pyrrole](1529806-92-5)

Safety Data

• Hazardous Substances Data: 1529806-92-5(Hazardous Substances Data)

Upstream product

• 1584210-03-6 3-(2-methyl-1-tosylaziridin-2-yl)prop-2-yn-1-ol 
• 1584221-47-5 C₂₃H₂₁ClN₂O₂S 
• 78-80-8 2-methylbut-1-en-3-yne 
• 55962-05-5 [N-(p-tolylsulfonyl)imino]phenyliodinane 
• 1529806-73-2 N-((1-benzyl-6-chloro-1H-indol-2-yl)methyl)-4-methyl-N-(3-(2-methyl-1-tosylaziridin-2-yl)-prop-2-ynyl)benzenesulfonamide 
• 1584209-01-7 2-(3-(tert-butyldimethylsilyloxy)prop-1-yn-1-yl)-2-methyl-1-tosylaziridine 
• 1584206-86-9 tert-butyldimethyl(4-methylpent-4-en-2-ynyloxy)silane 
• 10605-68-2 4-methyl-4-penten-2-yn-1-ol 
• 1584221-46-4 C₂₃H₁₉ClN₂O₂S 
• 70-55-3 toluene-4-sulfonamide 
• 1584221-45-3 C₁₆H₁₂ClNO 
• 1584221-43-1 C₁₆H₁₄ClNO 
• 1584221-42-0 C₁₇H₁₄ClNO₂ 
• 98081-84-6 6-chloro-2-methoxycarbonylindole 

Relevant articles and documents

Gold(I)-catalyzed rearrangement of alkynylaziridine indoles for the synthesis of spiro-tetrahydro-β-carbolines

Functionalized spiro-tetrahydro-β-carbolines were formed by an efficient gold(I)-catalyzed rearrangement reaction of alkynylaziridine indoles. The reaction involved a Friedel-Crafts type intramolecular reaction of alkynylaziridine indoles, following by hydroamination of aminoallene intermediate.