69819-53-0

Basic information

• Product Name: N-[(E)-2-Furylmethylidene]-2-phenylethanamine
• Synonyms: N-[(E)-2-Furylmethylidene]-2-phenylethanamine
• CAS NO: 69819-53-0
• Molecular Formula: C₁₃H₁₃NO
• Molecular Weight: 199.25
• Mol File: 69819-53-0.mol
• Article Data: 8

Chemical Properties

• Appearance: /
• CAS DataBase Reference: N-[(E)-2-Furylmethylidene]-2-phenylethanamine(CAS DataBase Reference)
• NIST Chemistry Reference: N-[(E)-2-Furylmethylidene]-2-phenylethanamine(69819-53-0)
• EPA Substance Registry System: N-[(E)-2-Furylmethylidene]-2-phenylethanamine(69819-53-0)

Safety Data

• Hazardous Substances Data: 69819-53-0(Hazardous Substances Data)

Upstream product

• 98-01-1 furfural 
• 64-04-0 phenethylamine 

Downstream Products

• 4439-55-8 N-(furan-2-ylmethyl)-2-phenylethan-1-amine 
• 77960-22-6 4-oxo-3-phenethyl-10-oxa-3-azatricyclo[5.2.1.0^1,5]dec-8-ene-6-carboxylic acid 
• 943251-45-4 3-oxo-2-phenethyl-2,3-dihydro-1H-isoindole-5-carboxylic acid 
• 1403502-02-2 bis(N-furfuryl-N-(2-phenylethyl)dithiocarbamato-S,S')lead(II) 
• 1429934-24-6 C₂₈H₂₈N₂O₂S₄Zn 
• 1429934-27-9 C₃₈H₃₆N₄O₂S₄Zn 

Relevant articles and documents

Volatiles from the Psychrotolerant Bacterium Chryseobacterium polytrichastri

The flavobacterium Chryseobacterium polytrichastri was investigated for its volatile profile by use of a closed-loop stripping apparatus (CLSA) and subsequent GC-MS analysis. The analyses revealed a rich headspace extract with 71 identified compounds. Compound identification was based on a comparison to library mass spectra for known compounds and on a synthesis of authentic standards for unknowns. Important classes were phenylethyl amides and a series of corresponding imines and pyrroles.

Synthesis, spectral and X-ray structural studies on Hg(II) dithiocarbamate complexes: A new precursor for HgS nanoparticles

Bis(N-furfuryl-N-(2-phenylethyl)dithiocarbamato-S,S′)mercury(II) (1), bis((furan-2-yl)methyl(2-(thiophen-2-yl)ethyl)dithiocarbamato-S,S′)mercury(II) (2), bis(N-benzyl-N-(2-(thiophen-2-yl)ethyl)dithiocarbamato-S,S′)mercury(II) (3) and bis(N-furfuryl-N-prop

Synthesis and spectral studies on Pb(II) dithiocarbamate complexes containing benzyl and furfuryl groups and their use as precursors for PbS nanoparticles

Nine lead bis(dithiocarbamate) complexes based on benzyl and furfuryl groups have been prepared. The complexes were characterized using IR and NMR spectroscopy. All the complexes showed the expected signals in 1H and 13C NMR spectra associated with the dithiocarbamate ligands. IR and 13C NMR spectral studies indicate that the S2CN double bond character increases with increase in length of alkyl chain bonded to nitrogen atom. Bis(N-benzyl-N-(2-phenylethyl)dithiocarbamato-S,S′)lead(II) (3) and bis(N-furfuryl-N-(2-phenylethyl)dithiocarbamato-S,S′)lead(II) (4) have been used as single source precursors for the synthesis of ethylenediamine capped PbS nanoparticles. Powder X-ray diffraction (PXRD), scanning electron microscopy (SEM), FTIR, UV-vis and fluorescence spectroscopy have been used to characterize the as-prepared lead sulfide nanoparticles. The PXRD measurements suggest that PbS nanoparticles are single phase with face-centered-cubic structure.