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About This Item
Linear Formula:
C10H7CHO
CAS Number:
Molecular Weight:
156.18
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
200-633-4
Beilstein/REAXYS Number:
386082
MDL number:
Product Name
1-Naphthaldehyde, 95%
InChI
1S/C11H8O/c12-8-10-6-3-5-9-4-1-2-7-11(9)10/h1-8H
InChI key
SQAINHDHICKHLX-UHFFFAOYSA-N
SMILES string
[H]C(=O)c1cccc2ccccc12
vapor density
>1 (vs air)
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.)
Quality Level
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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
signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral
Storage Class
10 - Combustible liquids
wgk
WGK 3
ppe
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
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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
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
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)
Highly enantioselective addition of dimethylzinc to arylaldehydes catalyzed by (2S)-1-ferrocenyl-methylaziridin-2-yl (diphenyl) methanol.
Wang M, et al.
Tetrahedron Asymmetry, 20(3), 288-292 (2009)
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