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525928

Sigma-Aldrich

Quinaldoyl chloride

97%

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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

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’.

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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)

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