46397-90-4

Basic information

• Product Name: N-ethyl-N-(1H-indol-3-ylmethyl)ethanamine
• Synonyms: 1H-Indole-3-methanamine, N,N-diethyl-; Diethyl-(1H-indol-3-ylmethyl)-amine; N-Ethyl-N-(1H-indol-3-ylmethyl)ethanamine
• CAS NO: 46397-90-4
• Molecular Formula: C₁₃H₁₈N₂
• Molecular Weight: 202.2954
• Mol File: 46397-90-4.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 324.5°C at 760 mmHg
• Flash Point: 150°C
• Density: 1.056g/cm³
• Vapor Pressure: 0.000245mmHg at 25°C
• Refractive Index: 1.602
• CAS DataBase Reference: N-ethyl-N-(1H-indol-3-ylmethyl)ethanamine(CAS DataBase Reference)
• NIST Chemistry Reference: N-ethyl-N-(1H-indol-3-ylmethyl)ethanamine(46397-90-4)
• EPA Substance Registry System: N-ethyl-N-(1H-indol-3-ylmethyl)ethanamine(46397-90-4)

Safety Data

• Hazardous Substances Data: 46397-90-4(Hazardous Substances Data)

Upstream product

• 83234-91-7 N-((1H-indol-1-yl)methyl)-N-ethylethanamine 

Downstream Products

• 64258-95-3 ethyl 2-formamido-3-(3-indolyl)-2-carbethoxypropionate 
• 132515-49-2 3-(benzoylaminomethyl)indole 
• 87-51-4 indole-3-acetic acid 
• 102664-68-6 1,3-bis-(benzoylamino-methyl)-indole 
• 487-89-8 Indole-3-carboxaldehyde 
• 10184-98-2 diethyl 2-[(1H-indol-3-yl)methyl]malonate 
• 1313529-92-8 4-(1-methyl-1H-indol-3-yl)-3-(3,4,5-trimethoxyphenyl)-1H-pyrazol-5-amine 
• 1313529-96-2 2-(1-methyl-1H-indol-3-yl)-3-oxo-3-(3,4,5-trimethoxyphenyl)propanenitrile 
• 1313529-95-1 8-(1-methyl-1H-indol-3-yl)-7-(3,4,5-trimethoxyphenyl)pyrazolo[1,5-a][1,3,5]triazine-2,4(1H,3H)-dione 
• 1313529-94-0 3-(1-methyl-1H-indol-3-yl)-5,7-bis(trifluoromethyl)-2-(3,4,5-trimethoxyphenyl)pyrazolo[1,5-a]pyrimidine 
• 1313530-01-6 N-(4-(1-methyl-1H-indol-3-yl)-3-(3,4,5-trimethoxyphenyl)-1H-pyrazol-5-yl)methanesulfonamide 
• 1313529-98-4 2,2,2-trifluoro-N-(4-(1-methyl-1H-indol-3-yl)-3-(3,4,5-trimethoxyphenyl)-1H-pyrazol-5-yl)acetamide 
• 771-51-7 indole-3-acetonitrile 
• 54-12-6 Trp 

Relevant articles and documents

Hf(OTf)4-Catalyzed regioselective N -aminomethylation of indoles and related NH-containing heterocycles

Figure presented Under Lewis acidic conditions using Hf(OTf)4, the aminomethylation of an indole derivative with a typical N,O-acetal preferentially produced kinetically favored N-aminomethylated indole derivatives instead of thermodynamically favored 3-aminomethylated indoles.