N109
1-Naphthaldehyde
95%
Synonym(s):
α-Naphthal, Naphthalene-1-carbaldehyde, α-Naphthaldehyde
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About This Item
Linear Formula:
C10H7CHO
CAS Number:
Molecular Weight:
156.18
Beilstein:
386082
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Recommended Products
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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Transformation of schiff bases derived from alpha?naphthaldehyde. Synthesis, spectral data and biological activity of new?3?aryl?2?(??naphtyl)?4?thiazolidinones and N?aryl?N?[1?(??naphthyl) but?3?enyl] amines.
Kouznetsov V, et al.
Journal of Heterocyclic Chemistry, 41(6), 995-999 (2004)
Miraç Ocak et al.
Journal of fluorescence, 27(1), 59-68 (2016-09-17)
Four new Schiff base ligands carrying naphthalene groups were prepared from the reaction of 2,4-diamino-6-methyl-1,3,5-triazine and 2,4-diamino-6-undecyl-1,3,5-triazine with 2-hydroxy-1-naphthaldehyde. The influence of a series of metal ions including Cu
NHC catalyzed oxidations of aldehydes to esters: chemoselective acylation of alcohols in presence of amines.
De Sarkar S, et al.
Journal of the American Chemical Society, 132(4), 1190-1191 (2010)
Carl A Busacca et al.
Magnetic resonance in chemistry : MRC, 48(1), 74-79 (2009-10-08)
Three isomeric o-fluoronaphthaldehydes, 9-fluorophenanthrene, and three previously unreported o-fluorophenanthrene aldehydes were analyzed in detail by multiple NMR techniques to provide unambiguous assignment of structures and resonances. The six aldehydes serve as the key starting materials for novel chiral ligands used
V Krishnakumar et al.
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
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