Date published: 2025-9-25

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2-Chloroquinoline (CAS 612-62-4)

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CAS Number:
612-62-4
Molecular Weight:
163.60
Molecular Formula:
C9H6ClN
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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2-Chloroquinoline is a key chemical compound in the quinoline family, distinguished by its aromatic heterocyclic structure where a benzene ring is fused with a pyridine ring, and a chlorine atom is substituted at the second position. This chlorination enhances its reactivity, making it a valuable intermediate in the synthesis of complex quinoline derivatives used across various industries, including pharmaceuticals, agrochemicals, and dye manufacturing. In chemical research, 2-chloroquinoline is particularly pivotal for facilitating nucleophilic substitution reactions, essential for creating advanced organic molecules. It also plays a crucial role in enabling cross-coupling reactions like Suzuki and Heck reactions, which are instrumental in generating new compounds with potential applications in materials science and catalysis. The unique properties of 2-chloroquinoline, such as the electron-withdrawing effect of the chlorine atom, allow for detailed studies of electrophilic and nucleophilic substitution mechanisms, significantly contributing to the broader understanding of heterocyclic chemistry and enhancing the development of tailored chemical entities for specific functional uses in diverse scientific and industrial domains.


2-Chloroquinoline (CAS 612-62-4) References

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  4. Synthesis and 3D-QSAR analysis of 2-chloroquinoline derivatives as H37 RV MTB inhibitors.  |  Khunt, RC., et al. 2013. Chem Biol Drug Des. 82: 669-84. PMID: 23790070
  5. Synthesis and biological evaluation of new rhodanine analogues bearing 2-chloroquinoline and benzo[h]quinoline scaffolds as anticancer agents.  |  Ramesh, V., et al. 2014. Eur J Med Chem. 83: 569-80. PMID: 24996143
  6. Regioselective synthesis of 2-chloroquinoline based ethyl 4-(3- hydroxyphenyl)-2,7,7-trimethyl-5-oxo-1,4,5,6,7,8-hexahydroquinoline-3- carboxylates and their in-silico evaluation against P. falciparum lactate dehydrogenase.  |  Rajesh, K., et al. 2015. Med Chem. 11: 789-97. PMID: 25925671
  7. Mutagenicities of quinoline and its derivatives.  |  Nagao, M., et al. 1977. Mutat Res. 42: 335-42. PMID: 323699
  8. Toluene Dioxygenase-Catalyzed cis-Dihydroxylation of Quinolines: A Molecular Docking Study and Chemoenzymatic Synthesis of Quinoline Arene Oxides.  |  Boyd, DR., et al. 2020. Front Bioeng Biotechnol. 8: 619175. PMID: 33644006
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Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

2-Chloroquinoline, 1 g

sc-256125
1 g
$48.00

2-Chloroquinoline, 5 g

sc-256125A
5 g
$121.00