442531-80-8

Basic information

• Product Name: N-[2-(1H-indol-3-yl)ethyl]-N,4-dimethylbenzenesulfonamide
• Synonyms: N-[2-(1H-indol-3-yl)ethyl]-N,4-dimethylbenzenesulfonamide
• CAS NO: 442531-80-8
• Molecular Formula: C₁₈H₂₀N₂O₂S
• Molecular Weight: 328.4286
• Mol File: 442531-80-8.mol
• Article Data: 3

Chemical Properties

• Appearance: /
• CAS DataBase Reference: N-[2-(1H-indol-3-yl)ethyl]-N,4-dimethylbenzenesulfonamide(CAS DataBase Reference)
• NIST Chemistry Reference: N-[2-(1H-indol-3-yl)ethyl]-N,4-dimethylbenzenesulfonamide(442531-80-8)
• EPA Substance Registry System: N-[2-(1H-indol-3-yl)ethyl]-N,4-dimethylbenzenesulfonamide(442531-80-8)

Safety Data

• Hazardous Substances Data: 442531-80-8(Hazardous Substances Data)

Upstream product

• 58635-45-3 methyl 2-(1-H-indol-3-yl)ethylcarbamate 
• 61-49-4 [2-(1H-indol-3-yl)-ethyl]-methylamine 
• 98-59-9 p-toluenesulfonyl chloride 
• 61-54-1 tryptamine 
• 6346-09-4 4-aminobutyrylaldehyde diethylacetal 
• 74-88-4 methyl iodide 
• 86658-78-8 N-tosyl tryptamine 

Downstream Products

• 1448523-02-1 N-(2-(1-allyl-1H-indol-3-yl)ethyl)-N,4-dimethylbenzenesulfonamide 
• 1448522-97-1 N-(2-(1-benzyl-2-oxoindolin-3-yl)ethyl)-N,4-dimethylbenzenesulfonamide 
• 1448523-00-9 N-(2-(1-allyl-2-oxoindolin-3-yl)ethyl)-N,4-dimethylbenzenesulfonamide 
• 1448523-03-2 (-)-N-(2-((S)-1-allyl-3-((3aS,3'aR,8aS,8'aS)-8'-allyl-1,1'-dimethyl-2,2',3,3',8,8a,8',8'a-octahydro-1H,1'H-[3a,3'a-bipyrrolo[2,3-b]indol]-7-yl)-2-oxoindolin-3-yl)ethyl)-N,4-dimethylbenzenesulfonamide 
• 857776-34-2 N-(2-(1-benzyl-1H-indol-3-yl)ethyl)-N,4-dimethylbenzenesulfonamide 
• 61-49-4 [2-(1H-indol-3-yl)-ethyl]-methylamine 

Relevant articles and documents

Unified Approach to the Spiro(pyrrolidinyl-oxindole) and Hexahydropyrrolo[2,3-b]indole Alkaloids: Total Syntheses of Pseudophrynamines 270 and 272A

The first enantioselective total syntheses of architecturally interesting prenylated pyrroloindole alkaloids, (-)-pseudophrynamines 272A (3d) and 270 (3b), have been achieved starting from enantioenriched 2-oxindoles having all-carbon quaternary stereocenters. A common strategy involving a thio-urea catalyzed aldol reaction is employed for the total synthesis of both spiro(pyrrolidinyl-oxindole) and hexahydropyrrolo[2,3-b]indole alkaloids.

Biogenetic-type synthesis of the Calycanthaceous alkaloids.

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