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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)-

2-Pyridinecarboxylic acid, 4,6-dichloro-, methyl ester

COC(=O)c1cc(Cl)cc(n1)Cl Request for Quotation
Chemical Name: 2-Pyridinecarboxylic acid, 4,6-dichloro-, methyl ester
CAS Number: 98273-19-9
Product Number: AG0035WT(AGN-PC-0229FU)
Synonyms:
MDL No:
Molecular Formula: C7H5Cl2NO2
Molecular Weight: 206.0261

Identification/Properties

Properties
Storage:
Inert atmosphere;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
206.022g/mol
XLogP3:
2.6
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
2
Exact Mass:
204.97g/mol
Monoisotopic Mass:
204.97g/mol
Topological Polar Surface Area:
39.2A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
177
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:
H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


Methyl 4,6-dichloropicolinate is a versatile compound commonly used in chemical synthesis as a key intermediate in the production of various organic compounds. This compound serves as a valuable building block in the creation of pharmaceuticals, agrochemicals, and specialty chemicals due to its unique chemical properties. Its presence enables the introduction of specific functional groups and structural motifs into target molecules, allowing for the development of novel chemical entities with desired properties. In addition, Methyl 4,6-dichloropicolinate plays a crucial role in the development of new materials and research in the field of organic chemistry. Its strategic placement within synthetic pathways contributes to the efficient and selective formation of complex molecules, making it an essential component in the modern chemical synthesis toolbox.