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4-Chloroquinoline, 99%|446659|611-35-8

4-Chloroquinoline, 99%

Cat. No JK446659_5_G
J&K Chemical

Product Information

Product Name
4-Chloroquinoline, 99%
Brand Name
J&K
Product Number
446659
CAS
611-35-8
Molecular Formula
C9H6ClN
Molecular Weight
163.61
Certificate of Analysis (COA)​
COA not found

General Information

PubChem CID
69140
IUPAC Name
4-chloroquinoline
InChI Key
KNDOFJFSHZCKGT-UHFFFAOYSA-N
SMILES
C1=CC=C2C(=C1)C(=CC=N2)Cl

Properties

Density
1.25
Melting Point
28-31
Boiling Point
260-261
Flash Point
110

Safety Information

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

Reactions with Alkenes
Publication Name: Science of Synthesis
Publication Date: 2026

Facile synthesis of novel quinolin-8-amine derivatives: crystallographic study, in silico and antifungal investigation
Publication Name: Chemical and Biological Technologies in Agriculture
Publication Date: 2025-09-26
DOI: 10.1186/s40538-025-00853-4

Synthesis, antimicrobial evaluation, and in silico studies of some novel hydrazinylquinoline and pyrazoline derivatives as potential antimicrobial agents
Publication Name: Future Journal of Pharmaceutical Sciences
Publication Date: 2025-09-25
DOI: 10.1186/s43094-025-00882-8

SMYD family in cancer: epigenetic regulation and molecular mechanisms of cancer proliferation, metastasis, and drug resistance
Publication Name: Experimental & Molecular Medicine
Publication Date: 2024-11-01
DOI: 10.1038/s12276-024-01326-8

Palladium-catalysed methylene C(sp 3)-H lactamization and cycloamination enabled by chlorinated pyridine-pyridone ligands
Publication Name: Nature Synthesis
Publication Date: 2024-04-11
DOI: 10.1038/s44160-024-00517-5

4-Chloroquinoline, 99%

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