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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 2-bromo-4-chloropyridine-3-carboxylate

CCOC(=O)c1c(Cl)ccnc1Br Request for Quotation
Chemical Name: ethyl 2-bromo-4-chloropyridine-3-carboxylate
CAS Number: 1256561-52-0
Product Number: AG000O9L(AGN-PC-0D0E8I)
Synonyms:
MDL No:
Molecular Formula: C8H7BrClNO2
Molecular Weight: 264.5037

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 2-bromo-4-chloronicotinate is a versatile compound that finds widespread application in chemical synthesis. This compound serves as a key building block in the creation of various pharmaceuticals, agrochemicals, and advanced materials. Its unique molecular structure imparts valuable reactivity and specificity in organic reactions, making it a valuable tool for chemists and researchers alike.In chemical synthesis, Ethyl 2-bromo-4-chloronicotinate is often utilized as a precursor in the preparation of complex molecules through functional group transformations. Its bromo and chloro substituents enable selective derivatization at specific positions, allowing for the controlled synthesis of diverse chemical entities. Additionally, the ethyl ester moiety provides a handle for further modifications, facilitating the creation of novel compounds with tailored properties.Furthermore, Ethyl 2-bromo-4-chloronicotinate plays a crucial role in the development of new pharmaceuticals and bioactive molecules. By incorporating this compound into molecular frameworks, researchers can explore structure-activity relationships and design analogs with enhanced biological activities. Its presence in drug discovery projects underscores its importance as a strategic intermediate in medicinal chemistry endeavors.Overall, Ethyl 2-bromo-4-chloronicotinate serves as a valuable tool for chemists engaging in organic synthesis, enabling the construction of intricate molecular architectures with precision and efficiency. Its diverse applications highlight its significance in advancing the frontiers of chemical research and innovation.