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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 4-bromo-6-chloronicotinate

CCOC(=O)c1cnc(cc1Br)Cl Request for Quotation
Chemical Name: Ethyl 4-bromo-6-chloronicotinate
CAS Number: 1807221-07-3
Product Number: AG01FS2Z(AGN-PC-3H5PO8)
Synonyms:
MDL No:
Molecular Formula: C8H7BrClNO2
Molecular Weight: 264.5037

Identification/Properties

Computed Properties
Molecular Weight:
264.5g/mol
XLogP3:
2.7
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
3
Exact Mass:
262.93487g/mol
Monoisotopic Mass:
262.93487g/mol
Topological Polar Surface Area:
39.2Ų
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
191
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

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 4-bromo-6-chloronicotinate is a versatile chemical compound widely used in chemical synthesis for various applications. It serves as a key building block in the production of pharmaceuticals, agrochemicals, and advanced materials due to its unique structural characteristics. In organic synthesis, this compound can undergo numerous reactions, including substitution, cross-coupling, and functional group interconversion, to create structurally diverse and complex molecules. Its presence in the synthesis of biological and pharmaceutical compounds highlights its importance in drug discovery and development processes. Additionally, the distinct bromo and chloro substituents offer opportunities for further derivatization to tailor the compound for specific applications, making it a valuable tool in the hands of synthetic chemists.