56999-26-9

Basic information

• Product Name: N-benzyl-2-(1-methyl-1H-indol-3-yl)acetamide
• CAS NO: 56999-26-9
• Molecular Formula: C₁₈H₁₈N₂O
• Molecular Weight: 278.3483
• Mol File: 56999-26-9.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 549.5°C at 760 mmHg
• Flash Point: 286.2°C
• Density: 1.11g/cm³
• Vapor Pressure: 3.98E-12mmHg at 25°C
• Refractive Index: 1.603
• CAS DataBase Reference: N-benzyl-2-(1-methyl-1H-indol-3-yl)acetamide(CAS DataBase Reference)
• NIST Chemistry Reference: N-benzyl-2-(1-methyl-1H-indol-3-yl)acetamide(56999-26-9)
• EPA Substance Registry System: N-benzyl-2-(1-methyl-1H-indol-3-yl)acetamide(56999-26-9)

Safety Data

• Hazardous Substances Data: 56999-26-9(Hazardous Substances Data)

Upstream product

• 300394-71-2 (1-methyl-indol-3-yl)-acetic acid hydrazide 
• 73031-14-8 2-(1H-indol-3-yl)-N-benzyl acetamide 
• 74-88-4 methyl iodide 
• 1477-49-2 3-indolylglyoxylic acid 
• 87-51-4 indole-3-acetic acid 
• 120-72-9 indole 
• 19260-05-0 1-methylgramine methiodide 
• 1912-48-7 2-(1-methyl-1H-indol-3-yl)acetic acid 
• 58665-00-2 (1-methyl-1H-indol-3-yl)acetic acid methyl ester 
• 100-46-9 benzylamine 

Downstream Products

• 1383933-54-7 ethyl 3-((3aS,8aR)-1-benzyl-8-methyl-2-oxo-1,2,3,3a,8,8a-hexahydropyrrolo[2,3-b]indol-3a-yl)benzoate 
• 1383933-56-9 (3aS,8aR)-1-benzyl-3a-(3-bromophenyl)-8-methyl-3,3a,8,8a-tetrahydropyrrolo[2,3-b]indol-2(1H)-one 
• 1383933-43-4 (3aS,8aR)-1-benzyl-8-methyl-3a-p-tolyl-3,3a,8,8a-tetrahydropyrrolo[2,3-b]indol-2(1H)-one 
• 1383933-44-5 (3aS,8aR)-1-benzyl-3a-(4-methoxyphenyl)-8-methyl-3,3a,8,8a-tetrahydropyrrolo[2,3-b]indol-2(1H)-one 
• 1383933-46-7 (3aS,8aR)-1-benzyl-3a-(biphenyl-4-yl)-8-methyl-3,3a,8,8a-tetrahydropyrrolo[2,3-b]indol-2(1H)-one 
• 1383933-48-9 (3aS,8aR)-1-benzyl-3a-(4-chlorophenyl)-8-methyl-3,3a,8,8a-tetrahydropyrrolo[2,3-b]indol-2(1H)-one 
• 1383933-50-3 (3aS,8aR)-1-benzyl-3a-(4-bromophenyl)-8-methyl-3,3a,8,8a-tetrahydropyrrolo[2,3-b]indol-2(1H)-one 
• 1383933-52-5 (3aS,8aR)-1-benzyl-8-methyl-3a-(4-(trifluoromethyl)phenyl)-3,3a,8,8atetrahydropyrrolo[2,3-b]indol-2(1H)-one 
• 1383933-62-7 (3aR,8aR)-1-benzyl-3a-(2-methoxyphenyl)-8-methyl-3,3a,8,8a-tetrahydropyrrolo[2,3-b]indol-2(1H)-one 
• 1383933-64-9 (3aR,8aR)-1-benzyl-8-methyl-3a-(thiophen-3-yl)-3,3a,8,8a-tetrahydropyrrolo[2,3-b]indol-2(1H)-one 
• 1383933-58-1 (3aS,8aR)-1-benzyl-8-methyl-3a-(naphthalen-2-yl)-3,3a,8,8a-tetrahydropyrrolo[2,3-b]indol-2(1H)-one 
• 1383933-60-5 (3aR,8aR)-1-benzyl-3a-(2-fluorophenyl)-8-methyl-3,3a,8,8a-tetrahydropyrrolo[2,3-b]indol-2(1H)-one 
• 1383933-39-8 (3aS,8aR)-1-benzyl-8-methyl-3a-phenyl-3,3a,8,8a-tetrahydropyrrolo[2,3-b]indol-2(1H)-one 
• 1383933-41-2 N-benzyl-2-(1-methyl-2-phenyl-1H-indol-3-yl)acetamide 

Relevant articles and documents

Enantioselective copper-catalyzed construction of aryl pyrroloindolines via an arylation-cyclization cascade

An enantioselective arylation-cyclization cascade has been accomplished using a combination of diaryliodonium salts and asymmetric copper catalysis. These mild catalytic conditions provide a new strategy for the enantioselective construction of pyrroloindolines, an important alkaloid structural motif that is commonly found among biologically active natural products.