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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-6-chloropyridine-3-carboxylate

CCOC(=O)c1cnc(c(c1)Br)Cl Request for Quotation
Chemical Name: ethyl 5-bromo-6-chloropyridine-3-carboxylate
CAS Number: 952063-30-8
Product Number: AG00IITS(AGN-PC-07QVKH)
Synonyms:
MDL No:
Molecular Formula: C8H7BrClNO2
Molecular Weight: 264.50368

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 5-bromo-6-chloronicotinate is a versatile compound, widely used in chemical synthesis as a key building block in the creation of various organic molecules. Its unique structure and reactivity make it an essential component in the formation of pharmaceuticals, agrochemicals, and materials.In chemical synthesis, Ethyl 5-bromo-6-chloronicotinate serves as a valuable intermediate for the production of complex organic compounds through various reactions such as nucleophilic substitution, transition metal-catalyzed cross-coupling, and aromatic substitution. Its bromo and chloro substituents enable a wide range of functionalization options, allowing chemists to tailor the molecule's properties for specific applications.This compound's role in chemical synthesis extends to the development of new drugs, where it can be utilized in the construction of biologically active molecules with potential therapeutic benefits. Additionally, Ethyl 5-bromo-6-chloronicotinate finds applications in the synthesis of advanced materials, including polymers and dyes, where its structural features impart desirable properties and functionalities.Overall, Ethyl 5-bromo-6-chloronicotinate plays a crucial role in the field of chemical synthesis, offering chemists a versatile building block for the creation of diverse organic compounds with practical applications across various industries.