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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)-

4-hydroxy-2-(2-pyridinyl)-5-pyrimidinecarboxylic acid

OC(=O)c1cnc(nc1O)c1ccccn1 Request for Quotation
Chemical Name: 4-hydroxy-2-(2-pyridinyl)-5-pyrimidinecarboxylic acid
CAS Number: 56406-45-2
Product Number: AG00EJ9U(AGN-PC-0OCDAH)
Synonyms:
MDL No:
Molecular Formula: C10H7N3O3
Molecular Weight: 217.1809

Identification/Properties

Properties
Storage:
Keep in dry area;2-8℃;
Computed Properties
Molecular Weight:
217.184g/mol
XLogP3:
0.5
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
2
Exact Mass:
217.049g/mol
Monoisotopic Mass:
217.049g/mol
Topological Polar Surface Area:
91.6A^2
Heavy Atom Count:
16
Formal Charge:
0
Complexity:
387
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:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


4-Hydroxy-2-(pyridin-2-yl)pyrimidine-5-carboxylic acid, also known as $name$, is a versatile compound widely utilized in chemical synthesis. This compound serves as a key building block in the production of various pharmaceuticals, agrochemicals, and materials due to its unique structural properties.In chemical synthesis, $name$ plays a crucial role as a heterocyclic intermediate in the preparation of biologically active compounds. Its functional groups enable it to participate in a range of reactions, such as nucleophilic substitution, condensation, and cyclization, leading to the formation of complex molecular structures with diverse applications.$name$ is particularly valued for its ability to serve as a linker or a ligand in coordination chemistry, facilitating the synthesis of metal complexes with enhanced catalytic or medicinal properties. Additionally, its presence in drug discovery and development processes has been instrumental in creating novel therapeutic agents with improved efficacy and safety profiles.Overall, the strategic incorporation of 4-Hydroxy-2-(pyridin-2-yl)pyrimidine-5-carboxylic acid in chemical synthesis strategies enables researchers to access a wide range of functionalized molecules with tailored properties for various industrial and scientific applications.