Skip to Content
Merck
All Photos(2)

Key Documents

525928

Sigma-Aldrich

Quinaldoyl chloride

97%

Sign Into View Organizational & Contract Pricing


About This Item

Empirical Formula (Hill Notation):
C10H6ClNO
CAS Number:
Molecular Weight:
191.61
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Assay

97%

mp

96-98 °C (dec.) (lit.)

storage temp.

2-8°C

SMILES string

ClC(=O)c1ccc2ccccc2n1

InChI

1S/C10H6ClNO/c11-10(13)9-6-5-7-3-1-2-4-8(7)12-9/h1-6H

InChI key

WFVMVMAUXYOQSW-UHFFFAOYSA-N

General description

Quinaldoyl chloride is a quinaldine derivative.

Application

Quinaldoyl chloride may be used to synthesize 5-chloro-2-(2-quinolinecarboxy)acetophenone and benzoin quinaldate.

Pictograms

Corrosion

Signal Word

Danger

Hazard Statements

Hazard Classifications

Skin Corr. 1B

Storage Class Code

8A - Combustible corrosive hazardous materials

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

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

Visit the Document Library

Synthesis of heterocyclic-substituted chromones and related compounds as potential anticancer agents.
D Donnelly et al.
Journal of medicinal chemistry, 8(6), 872-875 (1965-11-01)
Mechanism of the Acid Catalyzed Formation of Aldehydes from Reissert Compounds.
McEwen WE and Hazlett RN.
Journal of the American Chemical Society, 71(6), 1949-1952 (1949)

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