Key Documents

View All Documentation

250260

2-Naphthoyl chloride

Name: 2-Naphthoyl chloride
Brand: ALDRICH

98%

Synonym(s):

β-Naphthoyl chloride

Select a Size

Change View

About This Item

Linear Formula:

C₁₀H₇COCl

CAS Number:

2243-83-6

Molecular Weight:

190.63

UNSPSC Code:

12352100

NACRES:

NA.22

PubChem Substance ID:

24855046

EC Number:

218-822-5

Beilstein/REAXYS Number:

907776

MDL number:

MFCD00004093

Assay:

98%

Form:

solid

Technical Service

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

Let Us Assist

Properties

Quality Level

100

assay

98%

form

solid

bp

160-162 °C/11 mmHg (lit.)

mp

50-52 °C (lit.)

functional group

acyl chloride

SMILES string

ClC(=O)c1ccc2ccccc2c1

InChI

1S/C11H7ClO/c12-11(13)10-6-5-8-3-1-2-4-9(8)7-10/h1-7H

InChI key

XNLBCXGRQWUJLU-UHFFFAOYSA-N

Description

Application

2-Naphthoyl chloride has been used in:

preparation of amide derivatives of the amphetamine enantiomers
synthesis of 7-dimethylamino-2-methyl-3-naphthamido-phenothiazinium salt
modification of self-assembled monolayer formed on silica surface from ((((aminoethyl)amino)-methyl)phenethyl)trimethoxysilane

pictograms

GHS05

signalword

Danger

hcodes

H314

pcodes

P260 - P280 - P303 + P361 + P353 - P304 + P340 + P310 - P305 + P351 + P338 - P363

Hazard Classifications

Skin Corr. 1B

Storage Class

8A - Combustible corrosive hazardous materials

wgk

WGK 3

flash_point_f

235.4 °F - closed cup

flash_point_c

113 °C - closed cup

ppe

Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges

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

Liquid chromatographic chiral stationary phases in pharmaceutical analysis: determination of trace amounts of the (-)-enantiomer in (+)-amphetamine.

I W Wainer et al.

Journal of pharmaceutical sciences, 73(8), 1162-1164 (1984-08-01)

A rapid and accurate method was developed for the determination of the enantiomeric composition of amphetamine preparations. Amide derivatives of the amphetamine enantiomers are first formed by using achiral 2-naphthoyl chloride. The resulting enantiomeric amides are then chromatographed on a

Formation and naphthoyl derivatization of aromatic aminosilane self-assembled monolayers: characterization by atomic force microscopy and ultraviolet spectroscopy.

Durfor CN, et al.

Langmuir, 10(1), 148-152 (1994)

Full compositional control of PbSxSe1-x thin films by the use of acylchalcogourato lead(ii) complexes as precursors for AACVD.

Tagbo Emmanuel Ezenwa et al.

Dalton transactions (Cambridge, England : 2003), 47(47), 16938-16943 (2018-11-18)

Selenium and sulfur derivatives of lead(ii) acylchalcogourato complexes have been used to deposit PbSxSe1-x thin films by AACVD. By variation of the mole ratio of sulfur and selenium precursors in the aerosol feed solution the full range of compositions of

View All Related Papers

Global Trade Item Number

SKU	GTIN
250260-50G	04061831829020
250260-10G	04061825937359