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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, 1,6-dihydro-1-hydroxy-6-oxo-

OC(=O)c1cccc(=O)n1O Request for Quotation
Chemical Name: 2-Pyridinecarboxylic acid, 1,6-dihydro-1-hydroxy-6-oxo-
CAS Number: 94781-89-2
Product Number: AG005V95(AGN-PC-0NFMBK)
Synonyms:
MDL No:
Molecular Formula: C6H5NO4
Molecular Weight: 155.1082

Identification/Properties

Properties
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
155.109g/mol
XLogP3:
0.2
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
1
Exact Mass:
155.022g/mol
Monoisotopic Mass:
155.022g/mol
Topological Polar Surface Area:
77.8A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
266
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


1-Hydroxy-6-oxo-1,6-dihydropyridine-2-carboxylic acid, also known as $name$, is a versatile compound widely utilized in chemical synthesis as a key building block in organic reactions. This compound serves as a vital intermediate in the synthesis of various pharmaceuticals, agrochemicals, and fine chemicals due to its unique structural properties and reactivity. It plays a crucial role in the creation of complex molecules through its ability to undergo diverse chemical transformations, including oxidation, reduction, and functional group interconversions. The presence of both a hydroxyl and a carboxylic acid functionality in its structure enables $name$ to participate in a range of organic reactions, making it a valuable tool for synthetic chemists in designing efficient pathways for the synthesis of novel compounds with potential therapeutic or industrial applications.