Key Documents

View All Documentation

N109

1-Naphthaldehyde

Name: 1-Naphthaldehyde
Brand: ALDRICH

95%

Synonym(s):

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

Select a Size

Change View

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

Assay:

95%

Form:

liquid

Technical Service

Need help? Our team of experienced scientists is here for you.

Let Us Assist

Properties

vapor density

>1 (vs air)

Quality Level

200

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

Description

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

GHS07

signalword

Warning

hcodes

H302

pcodes

P264 - P270 - P301 + P312 - P501

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

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)

Metal Complexation Properties of Schiff Bases Containing 1,3,5-Triazine Derived from 2-Hydroxy-1-Naphthaldehyde in Solution. A Simple Spectrofluorimetric Method to Determine Mercury (II).

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

Spectral studies on cobalt(II), nickel(II) and copper(II) complexes of naphthaldehyde substituted aroylhydrazones.

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

View All Related Papers

Global Trade Item Number

SKU	GTIN
N109-100G-A	04061837381027
N109-500G-A	04061837381041
N109-2G-A	04061837381034