N109
1-Naphthaldehyde
95%
Synonym(s):
α-Naphthal, Naphthalene-1-carbaldehyde, α-Naphthaldehyde
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About This Item
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vapor density
>1 (vs air)
Quality Level
Assay
95%
form
liquid
refractive index
n20/D 1.652 (lit.)
bp
160-161 °C/15 mmHg (lit.)
mp
1-2 °C (lit.)
density
1.15 g/mL at 25 °C (lit.)
SMILES string
[H]C(=O)c1cccc2ccccc12
InChI
1S/C11H8O/c12-8-10-6-3-5-9-4-1-2-7-11(9)10/h1-8H
InChI key
SQAINHDHICKHLX-UHFFFAOYSA-N
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Application
1-Naphthaldehyde can be used to synthesize:
- (S)-1-α-naphthyl-1-ethanol
- N-(4-aryl)-N-(α-naphthyliden)amines
- N-aryl-N-[1-(1-naphthyl)but-3-enyl]amines
- naphthalene-1-carboxylic acid methyl ester
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 4 Oral
Storage Class Code
10 - Combustible liquids
WGK
WGK 3
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 69(2), 528-533 (2007-06-08)
The mid and far FTIR and Raman spectra were measured in the liquid state. The fundamental vibrational frequencies and intensity of vibrational bands were evaluated using density functional theory (DFT) and standard B3LYP/6-311+G** basis set combination. The vibrational spectra were
Highly enantioselective addition of dimethylzinc to arylaldehydes catalyzed by (2S)-1-ferrocenyl-methylaziridin-2-yl (diphenyl) methanol.
Tetrahedron Asymmetry, 20(3), 288-292 (2009)
Cytotoxic and Antifungal Activities of Diverse ?-Naphthylamine Derivatives.
Scientia Pharmaceutica, 80(4), 867-878 (2012)
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 64(4), 853-858 (2006-03-15)
A series of new coordination complexes of cobalt(II), nickel(II) and copper(II) with two new aroylhydrazones, 2-hydroxy-1-naphthaldehyde isonicotinoylhydrazone (H(2)L(1)) and 2-hydroxy-1-naphthaldehyde-2-thenoyl-hydrazone (H(2)L(2)) have been synthesized and characterized by elemental analysis, conductance measurements, magnetic susceptibility measurements, (1)H NMR spectroscopy, IR spectroscopy, electronic
NHC catalyzed oxidations of aldehydes to esters: chemoselective acylation of alcohols in presence of amines.
Journal of the American Chemical Society, 132(4), 1190-1191 (2010)
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