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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)-

3-Quinolinecarboxylic acid, 8-bromo-4-chloro-, ethyl ester

CCOC(=O)c1cnc2c(c1Cl)cccc2Br Request for Quotation
Chemical Name: 3-Quinolinecarboxylic acid, 8-bromo-4-chloro-, ethyl ester
CAS Number: 206258-97-1
Product Number: AG002IDS(AGN-PC-0KU2MY)
Synonyms:
MDL No:
Molecular Formula: C12H9BrClNO2
Molecular Weight: 314.5624

Identification/Properties

Properties
BP:
332.7°C at 760 mmHg
Storage:
Inert atmosphere;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
314.563g/mol
XLogP3:
3.7
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
3
Exact Mass:
312.951g/mol
Monoisotopic Mass:
312.951g/mol
Topological Polar Surface Area:
39.2A^2
Heavy Atom Count:
17
Formal Charge:
0
Complexity:
290
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information

NMR Spectrum

Other Analytical Data

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Chemical Structure


Ethyl 8-bromo-4-chloroquinoline-3-carboxylate is a versatile compound widely utilized in chemical synthesis as a key building block for the preparation of various pharmaceutical intermediates and active ingredients. Its unique structure and reactivity make it a valuable tool in the synthesis of complex organic molecules. Due to its bromo and chloro substituents, this compound can participate in a variety of key reactions such as nucleophilic substitution, palladium-catalyzed cross-coupling, and heterocycle formation. The presence of the quinoline ring further enhances its utility in medicinal chemistry, allowing for the modification of bioactive molecules. As a result, Ethyl 8-bromo-4-chloroquinoline-3-carboxylate is highly sought after by chemists and researchers involved in drug discovery and development, providing a crucial foundation for the creation of novel pharmaceutical compounds.