| Weight | 156.184 g/mol |
|---|---|
| Formula | C11H8O |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 1 |
2-Naphthaldehyde (66-99-9)
Score:
#1875 in Physics
,
#5834 in Chemistry
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- Crystal and molecular structure of 2-hydroxy-1-naphthaldehyde isonicotinoyl hydrazone (NIH) and its iron(III) complex: an iron chelator with anti-tumour activity (Journal of Biological Inorganic Chemistry, 1999)
- Intramolecular NH...O hydrogen bonding, quinoid effect, and partial -electron delocalization in N-aryl Schiff bases of 2-hydroxy-1-naphthaldehyde: the crystal structures of planar N-(-naphthyl)- and N-(-naphthyl)-2-oxy-1-naphthaldimine (Journal of Chemical Crystallography, 1996)
- Inhibition of the Ribonuclease H and DNA Polymerase Activities of HIV-1 Reverse Transcriptase by N-(4-tert-Butylbenzoyl)-2-hydroxy-1-naphthaldehyde Hydrazone (Biochemistry, 1997)
- Inner coordination sphere tin(IV) complexes with some O,N,N-terdentate {N-(2-hydroxybenzaldehyde)-1-amino-2-phenyleneimine and N-(2-hydroxy-1-naphthaldehyde)-1-amino-2-phenyleneimine} and O,N,N,O-quadridentate {N,N-bis(2-hydroxybenzaldehyde)-1,2-phenylenediimine and N,N-bis(2-hydroxy-1-naphthaldehyde)-1,2-phenylenediimine} Schiff bases (Polyhedron, 1997)
- Tautomerism in 2-hydroxy-1-naphthaldehyde schiff bases in solution and the solid state investigated using 13C NMR spectroscopy (Magnetic Resonance in Chemistry, 1993)
- Modulation of Excited-State Intramolecular Proton Transfer Reaction of 1-Hydroxy-2-naphthaldehyde in Different Supramolecular Assemblies (Langmuir, 2010)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1=CC=C2C=C(C=CC2=C1)C=O
-
InChIKeyPJKVFARRVXDXAD-UHFFFAOYSA-N
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