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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
Recommended Products
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.
Signal Word
Danger
Hazard Statements
Precautionary 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’.
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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)
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)
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