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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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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
Cytotoxic and Antifungal Activities of Diverse ?-Naphthylamine Derivatives.
Kouznetsov V, et al.
Scientia Pharmaceutica, 80(4), 867-878 (2012)
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)
Pramod Kumar Singh et al.
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
Magdalena Florek-Luszczki et al.
Epilepsy research, 108(10), 1728-1733 (2014-12-03)
The influence of WIN 55,212-2 mesylate (WIN) on the anticonvulsant activity and acute neurotoxic potential of clobazam (CLB) and lacosamide (LCM) was studied in the maximal electroshock-induced seizure (MES) model and chimney test in mice. indicate that WIN administered intraperitoneally
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