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525928

Quinaldoyl chloride

97%

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About This Item

Empirical Formula (Hill Notation):
C10H6ClNO
CAS Number:
50342-01-3
Molecular Weight:
191.61
NACRES:
NA.22
PubChem Substance ID:
24874521
UNSPSC Code:
12352100
MDL number:
MFCD02683554
Assay:
97%

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InChI

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

SMILES string

ClC(=O)c1ccc2ccccc2n1

InChI key

WFVMVMAUXYOQSW-UHFFFAOYSA-N

assay

97%

mp

96-98 °C (dec.) (lit.)

functional group

acyl chloride

storage temp.

2-8°C

Quality Level

200

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Quinaldoyl chloride 97%

Sigma-Aldrich

525928

Quinaldoyl chloride

2,6-Dichlorobenzenesulfonyl chloride 97%

Sigma-Aldrich

545708

2,6-Dichlorobenzenesulfonyl chloride

2-Oxo-1-imidazolidinecarbonyl chloride 96%

Sigma-Aldrich

524832

2-Oxo-1-imidazolidinecarbonyl chloride

Diethylthiocarbamoyl chloride 95%

Sigma-Aldrich

384291

Diethylthiocarbamoyl chloride

assay

97%

assay

97%

assay

96%

assay

95%

mp

96-98 °C (dec.) (lit.)

mp

53-56 °C (lit.)

mp

147-151 °C (lit.)

mp

45-50 °C (lit.)

storage temp.

2-8°C

storage temp.

-

storage temp.

-

storage temp.

-

functional group

acyl chloride

functional group

chloro

functional group

chloro

functional group

amine, chloro

General description

Quinaldoyl chloride is a quinaldine derivative.

Application

Quinaldoyl chloride may be used to synthesize 5-chloro-2-(2-quinolinecarboxy)acetophenone[1] and benzoin quinaldate.[2]

pictograms

Corrosion
GHS05

signalword

Danger

hcodes

H314

Hazard Classifications

Skin Corr. 1B

Storage Class

8A - Combustible corrosive hazardous materials

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

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

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Certificates of Analysis (COA)

Lot/Batch Number
0000289038
0000253666
0000240214
0000231428
0000240214

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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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