1591916-40-3

Basic information

• Product Name: C₁₆H₁₃ClINO₂S
• Synonyms: C₁₆H₁₃ClINO₂S
• CAS NO: 1591916-40-3
• Molecular Weight: 445.708
• Mol File: 1591916-40-3.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: C₁₆H₁₃ClINO₂S(CAS DataBase Reference)
• NIST Chemistry Reference: C₁₆H₁₃ClINO₂S(1591916-40-3)
• EPA Substance Registry System: C₁₆H₁₃ClINO₂S(1591916-40-3)

Safety Data

• Hazardous Substances Data: 1591916-40-3(Hazardous Substances Data)

Upstream product

• 1351706-37-0 N-(2-iodo-4-chlorophenyl)-4-methylbenzenesulfonamide 
• 106-96-7 propargyl bromide 
• 1591916-46-9 C₁₆H₁₃ClINO₂S 
• 63069-48-7 p-chloro-o-iodoaniline 
• 98-59-9 p-toluenesulfonyl chloride 

Relevant articles and documents

Palladium-Catalyzed Allenamide Carbopalladation/Allylation with Active Methine Compounds

A palladium-catalyzed allenamide carbopalladation/allylation with active methine compounds has been developed. Various indoles and isoquinolinones bearing a quaternary carbon center were achieved with good efficiency, a broad substrate scope and good functional group tolerance. This reaction underwent cascade oxidative addition, carbopalladation, and allylic alkylation, and two new C-C bonds were formed in one pot.

Asymmetric Domino Heck/Dearomatization Reaction of β-Naphthols to Construct Indole-Terpenoid Frameworks

A palladium-catalyzed enantioselective Heck cyclization/dearomatization cascade via capturing the cyclized Heck π-allylpalladium intermediate by β-naphthols is reported, which provides a new strategy for the construction of chiral indole-terpenoid framewo