Skip to Content
Merck
CN

N109

1-Naphthaldehyde

95%

Synonym(s):

α-Naphthal, Naphthalene-1-carbaldehyde, α-Naphthaldehyde

Sign In to View Organizational & Contract Pricing.

Select a Size

About This Item

Linear Formula:
C10H7CHO
CAS Number:
66-77-3
Molecular Weight:
156.18
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
24897459
EC Number:
200-633-4
Beilstein/REAXYS Number:
386082
MDL number:
MFCD00004003

Key Documents

View All Documentation
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist

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

200

Looking for similar products? Visit Product Comparison Guide

Related Categories

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

pictograms

Exclamation mark
GHS07

signalword

Warning

hcodes

H302

Hazard Classifications

Acute Tox. 4 Oral

Storage Class

10 - Combustible liquids

wgk

WGK 3

ppe

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
WXBF6935V
WXBF6059V
WXBF3882V
WXBD6870V
WXBF1547V

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Search for a COA

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

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)
View All Related Papers

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service