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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)-

ethyl 6-bromo-4-chloro-7-ethoxyquinoline-3-carboxylate

CCOC(=O)c1cnc2c(c1Cl)cc(c(c2)OCC)Br Request for Quotation
Chemical Name: ethyl 6-bromo-4-chloro-7-ethoxyquinoline-3-carboxylate
CAS Number: 953803-81-1
Product Number: AG00IJ0I(AGN-PC-0HXVIO)
Synonyms:
MDL No:
Molecular Formula: C14H13BrClNO3
Molecular Weight: 358.61492

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


Ethyl 6-bromo-4-chloro-7-ethoxyquinoline-3-carboxylate is a valuable compound that finds wide application in chemical synthesis. In the field of organic chemistry, this compound serves as a versatile building block for the construction of various complex molecules. Due to the presence of different functional groups such as bromo, chloro, ethoxy, and carboxylate on the quinoline ring, it can participate in a range of chemical reactions like substitution, esterification, and coupling reactions.One of the key applications of Ethyl 6-bromo-4-chloro-7-ethoxyquinoline-3-carboxylate lies in its utility as a precursor for the synthesis of biologically active compounds. By incorporating this compound into the structure of target molecules, researchers can modify the pharmacological properties of the resulting products. Additionally, this compound can be utilized in the development of new materials, pharmaceuticals, agrochemicals, and other specialty chemicals. Its strategic placement of functional groups allows for facile manipulation and derivatization, making it a valuable tool for synthetic chemists seeking to access diverse chemical space.