104876-48-4

Basic information

• Product Name: Acetamide, N-[1-[1-(phenylsulfonyl)-1H-indol-3-yl]ethenyl]-
• CAS NO: 104876-48-4
• Molecular Formula: C18H16N2O3S
• Molecular Weight: 340.403
• Mol File: 104876-48-4.mol

Chemical Properties

• CAS DataBase Reference: Acetamide, N-[1-[1-(phenylsulfonyl)-1H-indol-3-yl]ethenyl]-(CAS DataBase Reference)
• NIST Chemistry Reference: Acetamide, N-[1-[1-(phenylsulfonyl)-1H-indol-3-yl]ethenyl]-(104876-48-4)
• EPA Substance Registry System: Acetamide, N-[1-[1-(phenylsulfonyl)-1H-indol-3-yl]ethenyl]-(104876-48-4)

Safety Data

• Hazardous Substances Data: 104876-48-4(Hazardous Substances Data)

Upstream product

• 104876-46-2 N-<1-<1-(phenylsulfonyl)-1H-indol-3-yl>vinyl>diacetamide 
• 67-56-1 methanol 

Downstream Products

• 104876-50-8 (+/-)-N-<1-formyl-1β,2,3,9aβ-tetrahydro-9-(phenylsulfonyl)-9H-carbazol-4-yl>acetamide 
• 104876-51-9 4-(Acetylamino)-1,2,3,9a-tetrahydro-9-(phenylsulfonyl)-1-carbazolcarbonsaeure-methylester 
• 104876-52-0 4-(Acetylamino)-1,2,3,9a-tetrahydro-9-(phenylsulfonyl)-1-carbazolcarbonitril 
• 135862-15-6 (Z)-N-<1-<1-(phenylsulfonyl)-1H-indol-3-yl>-3,3,4,4-tetracyanobut-1-en-1-yl>acetamide 
• 135862-12-3 (+/-)-N-<1,2,3,3aβ,4,10,10aβ,10bβ-octahydro-1,3-dioxo-2-phenyl-10-(phenylsulfonyl)pyrrolo<3,4-a>carbazol-5-yl>acetamide 

Relevant articles and documents

Diels-Alder Reactions of (1H-Indol-3-yl)-enacetamides and -endiacetamides: A Selective Access to Acetylamino-Functionalized Annelated Indoles and Carbazoles

Diels-Alder reactions of the (1H-indol-3-yl)-enacetamides and -endiacetamides 1a - d with some carbodienophiles and 4-phenyl-3H-1,2,4-triazole-3,5(4H)-dione give rise to the novel amino-functionalized carbazoles 4 - 6 and 8 (Scheme 3).Ethenetetracarbonitrile reacts with 1b to furnish the Michael-type adduct 7 (Scheme 3).Structural aspects of the starting materials 1, which exhibit above all 3-vinyl-1H-indole reactivity, are discussed with regard to the prediction of a Diels-Alder process.

Indoles and Indole Alkaloids, XXI. - Preparation of 4-(Acetylamino)-1,2,3,9a-tetrahydrocarbazole Derivatives by Cycloadditions of 3-Indolyl-enimides and -enamides

Treatment of the oximes of the 3-acetylindoles 1 and 5 with acetic anhydride in pyridine results in the formation of the enimides 2 and 7, which slowly undergo cycloadditions with acrolein and derivatives of acrylic acid to form 3 and 10, respectively.Com