1584221-46-4

Basic information

• Product Name: C₂₃H₁₉ClN₂O₂S
• Synonyms: C₂₃H₁₉ClN₂O₂S
• CAS NO: 1584221-46-4
• Molecular Weight: 422.935
• Mol File: 1584221-46-4.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: C₂₃H₁₉ClN₂O₂S(CAS DataBase Reference)
• NIST Chemistry Reference: C₂₃H₁₉ClN₂O₂S(1584221-46-4)
• EPA Substance Registry System: C₂₃H₁₉ClN₂O₂S(1584221-46-4)

Safety Data

• Hazardous Substances Data: 1584221-46-4(Hazardous Substances Data)

Upstream product

• 1584221-45-3 C₁₆H₁₂ClNO 
• 70-55-3 toluene-4-sulfonamide 
• 1584221-43-1 C₁₆H₁₄ClNO 
• 1584221-42-0 C₁₇H₁₄ClNO₂ 
• 98081-84-6 6-chloro-2-methoxycarbonylindole 
• 98081-76-6 C₁₀H₈ClN₃O₂ 
• 104-88-1 4-chlorobenzaldehyde 

Downstream Products

• 1584221-47-5 C₂₃H₂₁ClN₂O₂S 
• 1529806-92-5 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] 
• 1529806-73-2 N-((1-benzyl-6-chloro-1H-indol-2-yl)methyl)-4-methyl-N-(3-(2-methyl-1-tosylaziridin-2-yl)-prop-2-ynyl)benzenesulfonamide 

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.