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2,6-Dichloroquinoline, 97%|317008|1810-72-6

2,6-Dichloroquinoline, 97%

Cat. No JK317008_5_G
J&K Chemical

Product Information

Product Name
2,6-Dichloroquinoline, 97%
Brand Name
J&K
Product Number
317008
CAS
1810-72-6
Molecular Formula
C9H5Cl2N
Molecular Weight
198.05
Certificate of Analysis (COA)​
COA not found

General Information

PubChem CID
607502
IUPAC Name
2,6-dichloroquinoline
InChI Key
LPDFGLZUUCLXGM-UHFFFAOYSA-N
SMILES
C1=CC2=C(C=CC(=N2)Cl)C=C1Cl

Properties

Melting Point
161-164

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

Co-catalyzed C–C Coupling Reactions with Csp2 Electrophiles
Publication Name: C-C Cross Couplings with 3d Base Metal Catalysts
Publication Date: 2023
DOI: 10.1007/3418_2023_89

Chromium-Catalyzed Cross-Coupling Reactions of Alkylmagnesium Reagents with Halo-Quinolines and Activated Aryl Chlorides
Publication Name: Synthesis
Publication Date: 2016-04-27
DOI: 10.1055/s-0035-1561615

A Monooxygenase Catalyzes Sequential Dechlorinations of 2,4,6-Trichlorophenol by Oxidative and Hydrolytic Reactions
Publication Name: The Journal of biological chemistry
Publication Date: 2004-02-20
DOI: 10.1074/jbc.m312072200

Cl35 nuclear quadrupole resonance spectra of chloro-substituted 6-pyridazone derivatives
Publication Name: Chemistry of Heterocyclic Compounds
Publication Date: 1976-03
DOI: 10.1007/bf00479578

2,6-Dichloroquinoline, 97%

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