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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(1H)-Pyridinone, 3-chloro-6-hydroxy-

Oc1ccc(c(=O)[nH]1)Cl Request for Quotation
Chemical Name: 2(1H)-Pyridinone, 3-chloro-6-hydroxy-
CAS Number: 103792-71-8
Product Number: AG007X4B(AGN-PC-0NVM9N)
Synonyms:
MDL No:
Molecular Formula: C5H4ClNO2
Molecular Weight: 145.5438

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Chemical Structure


3-Chloro-6-hydroxypyridin-2(1H)-one, also known as $name$, is a versatile compound widely used in chemical synthesis processes. This compound acts as an important building block in the creation of various pharmaceuticals, agrochemicals, and specialty chemicals. The presence of the hydroxyl group and the chlorine atom on the pyridine ring confers unique reactivity to this molecule, making it valuable in multiple synthetic pathways.One key application of 3-Chloro-6-hydroxypyridin-2(1H)-one is in the synthesis of heterocyclic compounds. By utilizing its specific functional groups, chemists can efficiently construct complex ring structures with desired properties. Additionally, this compound serves as a valuable intermediate in the production of pyridine derivatives, which are essential in the development of new drugs and agrochemicals.Furthermore, 3-Chloro-6-hydroxypyridin-2(1H)-one plays a crucial role in the preparation of chelating agents and ligands used in coordination chemistry. Its ability to coordinate with metal ions facilitates the formation of stable complexes, which find applications in catalysis and material science.Overall, the versatility and reactivity of 3-Chloro-6-hydroxypyridin-2(1H)-one make it a vital component in the toolbox of synthetic chemists, enabling the efficient construction of diverse molecular structures with tailored functions.