83824-09-3

Basic information

• Product Name: 1H-Indole-1-carboxaldehyde, 3-phenyl-
• CAS NO: 83824-09-3
• Molecular Formula: C15H11NO
• Molecular Weight: 221.258
• Mol File: 83824-09-3.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 1H-Indole-1-carboxaldehyde, 3-phenyl-(CAS DataBase Reference)
• NIST Chemistry Reference: 1H-Indole-1-carboxaldehyde, 3-phenyl-(83824-09-3)
• EPA Substance Registry System: 1H-Indole-1-carboxaldehyde, 3-phenyl-(83824-09-3)

Safety Data

• Hazardous Substances Data: 83824-09-3(Hazardous Substances Data)

Upstream product

• 1504-16-1 3-phenyl-1H-indole 
• 68-12-2 N,N-dimethyl-formamide 

Downstream Products

• 83824-20-8 N-(2,4-Dinitro-phenyl)-N'-[1-(3-phenyl-indol-1-yl)-meth-(E)-ylidene]-hydrazine 
• 83824-18-4 N-(4-Nitro-phenyl)-N'-[1-(3-phenyl-indol-1-yl)-meth-(E)-ylidene]-hydrazine 
• 30020-98-5 N-methyl-3-phenylindole 
• 95503-19-8 1-methyl-3-phenyl-3-(3'-phenylindolyl-1'-methyl)indoline 
• 95503-20-1 C₃₀H₂₄N₂O 

Relevant articles and documents

Synthesis and structural analysis of (e)-2-(2'-nitrovinyl)indoles from the corresponding 2-formylindole derivatives

Preparation of 2-formylindoles was carried out from the appropriate methylindole by oxidation with selenium dioxide and by Vilsmeier formylation. The 2-(2'-nitrovinyl)indoles have been obtained by condensation of 2-formylindoles with nitroalkanes in the presence of ammonium chloride in good yields. In this reaction, only the (E)-isomer of the 2-(2'-nitrovinyl)indoles was observed by 1H nmr and NOE experiments. Evidence for an extended conjugation through the double bond and the nitro group can be evaluate by the deshielding effect on the olefinic protons. Moreover, the non-Beer's law behaviour in the uv-visible spectra suggest the existence of some sort of complex for these compounds.

Pronounced Aldehydic Character of N-Formylindoles: Part II - Preparation, PMR and Mass Spectrometric Study of Their 4-Nitrophenyl- and 2,4-Dinitrophenyl-hydrazones

N-Formylindoles (1A-H) exhibit pronounced aldehydic character as revealed by the formation of 4-nitrophenylhydrazones (2A-E) and 2,4-dinitrophenylhydrazones (2F-J).The N-formylindoles (1E-G) bearing phenyl groups at 2- and 3-positions do not form either 4