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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)-

5-bromo-6-chloropyridine-2-carboxylic acid

OC(=O)c1ccc(c(n1)Cl)Br Request for Quotation
Chemical Name: 5-bromo-6-chloropyridine-2-carboxylic acid
CAS Number: 959958-25-9
Product Number: AG006TQS(AGN-PC-079GV6)
Synonyms:
MDL No:
Molecular Formula: C6H3BrClNO2
Molecular Weight: 236.4505

Identification/Properties

Properties
BP:
355.1±42.0°C at 760 mmHg
Storage:
Inert atmosphere;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
236.449g/mol
XLogP3:
2.4
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
1
Exact Mass:
234.904g/mol
Monoisotopic Mass:
234.904g/mol
Topological Polar Surface Area:
50.2A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
167
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#:
N/A
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


5-Bromo-6-chloropicolinic acid, a versatile chemical compound, plays a crucial role in chemical synthesis processes. This unique acid is commonly utilized as a building block in the production of various pharmaceuticals, agrochemicals, and advanced materials. Its distinctive properties make it a valuable reagent in organic synthesis, particularly in the formation of complex molecular structures. With its ability to participate in a wide range of chemical reactions, 5-Bromo-6-chloropicolinic acid serves as a key intermediate in the creation of diverse compounds with enhanced functionalities and properties. Its strategic placement within synthetic pathways enables the efficient construction of intricate molecules, making it indispensable in the field of modern chemistry.