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Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-
O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]
Tris(dibenzylideneacetone)dipalladium
C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C
Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

4-chloro-2-pyridin-2-ylquinoline

Clc1cc(nc2c1cccc2)c1ccccn1 Request for Quotation
Chemical Name: 4-chloro-2-pyridin-2-ylquinoline
CAS Number: 954225-55-9
Product Number: AG00IJ1X(AGN-PC-04TM1Q)
Synonyms:
MDL No:
Molecular Formula: C14H9ClN2
Molecular Weight: 240.68766

Identification/Properties

Safety Information

GHS Pictogram:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


4-Chloro-2-(pyridin-2-yl)quinoline, commonly referred to as $name$, serves as a versatile building block in chemical synthesis processes. This compound is frequently utilized as a key intermediate in the production of various pharmaceuticals, agrochemicals, and specialty chemicals due to its unique structure and reactivity. In organic synthesis, $name$ acts as a valuable precursor for the preparation of heterocyclic compounds, such as pyridine derivatives, by undergoing substitution, addition, or cyclization reactions. Its halogen and quinoline moieties play crucial roles in facilitating diverse transformations, enabling the synthesis of complex molecules with desired properties. Overall, the strategic incorporation of 4-Chloro-2-(pyridin-2-yl)quinoline in chemical reactions allows for the efficient and targeted construction of novel compounds with potential applications across different industries.