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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 5-bromo-2-chloropyridine-3-carboxylate

CCOC(=O)c1cc(Br)cnc1Cl Request for Quotation
Chemical Name: ethyl 5-bromo-2-chloropyridine-3-carboxylate
CAS Number: 1214332-67-8
Product Number: AG0014T6(AGN-PC-02M1Y6)
Synonyms:
MDL No:
Molecular Formula: C8H7BrClNO2
Molecular Weight: 264.5037

Identification/Properties

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
-
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


Ethyl 5-bromo-2-chloronicotinate is an essential building block in chemical synthesis, commonly used in the pharmaceutical and agrochemical industries. This compound serves as a versatile intermediate in the preparation of various biologically active molecules through organic reactions such as nucleophilic substitution, Suzuki coupling, and cross-coupling reactions. Its unique structure with both bromine and chlorine substituents imparts valuable properties that can be selectively modified to tailor the desired characteristics of the final product. In addition, Ethyl 5-bromo-2-chloronicotinate plays a crucial role in the development of potential drug candidates, pesticides, and other fine chemicals by serving as a key starting material for the synthesis of diverse heterocyclic compounds with significant biological activities.