Weight | 96.085 g/mol |
---|---|
Formula | C5H4O2 |
Hydrogen Acceptors | 2 |
Hydrogen Donors | 0 |
Aromatic Rings | 1 |
Rotatable Bonds | 1 |
3-Furaldehyde (498-60-2)
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- Structural and spectral studies of thiosemicarbazones derived from 3-furaldehyde and 3-(2-furyl)prop-2-enal (Journal of Molecular Structure, 2002)
- Structural and spectral studies of nickel(II), copper(II) and cadmium(II) complexes of 3-furaldehyde thiosemicarbazone (Polyhedron, 2005)
- Reactions of guaiazulene with 2-furaldehyde, thiophene-2-carbaldehyde and pyrrole-2-carbaldehyde in methanol in the presence of hexafluorophosphoric acid: comparative studies on molecular structures and spectroscopic, chemical and electrochemical properties of monocarbocations stabilized by 3-guaiazulenyl and 2-furyl (or 2-thienyl or 2-pyrrolyl) groups (Tetrahedron, 2005)
- Synthesis and spectroscopic studies on the Schiff base ligand derived from condensation of 2-furaldehyde and 3,3-diaminobenzidene, L and its complexes with Co(II), Ni(II), Cu(II) and Zn(II): Comparative DNA binding studies of L and its Cu(II) and Zn(II) complexes (Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy, 2011)
- Standard molar enthalpies of formation of 2-furancarbonitrile, 2-acetylfuran, and 3-furaldehyde (The Journal of Chemical Thermodynamics, 2009)
- Vapor-liquid equilibria for binary mixtures of butyl ether with 2-furaldehyde and with 2-, 3-, and 4-heptanone (Journal of Chemical & Engineering Data, 1988)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1=COC=C1C=O
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InChIKeyAZVSIHIBYRHSLB-UHFFFAOYSA-N
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