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2-Chloro-3-quinolinecarboxaldehyde, 98%|933690|73568-25-9

2-Chloro-3-quinolinecarboxaldehyde, 98%

Cat. No JK933690_5_G
J&K Chemical

Product Information

Product Name
2-Chloro-3-quinolinecarboxaldehyde, 98%
Brand Name
J&K
Product Number
933690
CAS
73568-25-9
Molecular Formula
C10H6ClNO
Molecular Weight
191.61
Certificate of Analysis (COA)​
COA not found

General Information

Synonyms
2-Chloroquinoline-3-carbaldehyde
PubChem CID
690958
IUPAC Name
2-chloroquinoline-3-carbaldehyde
InChI Key
SDKQWXCBSNMYBN-UHFFFAOYSA-N
SMILES
C1=CC=C2C(=C1)C=C(C(=N2)Cl)C=O

Properties

Density
1.364
Melting Point
148-152

Safety Information

GHS Symbols
Hazard Symbol
Signal Word
Warning
Hazard Statement
H315
H319
H335
Precautionary Statement
P280
P321
P261
P271
P319
P405
P501
P302+P352
P332+P317
P362+P364
P264+P265
P305+P351+P338
P337+P317
P304+P340
P403+P233

References Data Source From Pubchem

Synthesis, In Vitro Evaluation, Molecular Docking, and DFT Studies of Chitosan Aldehyde Derivatives as Anticancer Agents Via Modulation of the JNK/ERK-p53 Signaling Axis
Publication Name: Journal of Polymers and the Environment
Publication Date: 2026-02-20
DOI: 10.1007/s10924-025-03762-7

Catalyst-Assisted Synthesis of Benzimidazole Derivatives: Recent Advances and Mechanistic Insights
Publication Name: Topics in current chemistry (Cham)
Publication Date: 2026-01-03
DOI: 10.1007/s41061-025-00535-7

Synthetic exploration of quinoline-3-carbaldehyde in N,N-dimethylformamide
Publication Name: Journal of the Iranian Chemical Society
Publication Date: 2026-01
DOI: 10.1007/s13738-025-03305-w

Unleashing the Power of Vilsmeier–Haack Reaction in Synthesis of Heterocycles (A Review)
Publication Name: Russian Journal of Organic Chemistry
Publication Date: 2025-12
DOI: 10.1134/s1070428025602559

Dual role of ionic liquids in quinoline scaffolds syntheses: a green and sustainable perspective
Publication Name: Chemical Papers
Publication Date: 2025-10-13
DOI: 10.1007/s11696-025-04419-4

2-Chloro-3-quinolinecarboxaldehyde, 98%

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