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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-hydroxy-2-(hydroxymethyl)-3H-pyridin-4-one

OCC1=NC=C(C(=O)C1)O Request for Quotation
Chemical Name: 5-hydroxy-2-(hydroxymethyl)-3H-pyridin-4-one
CAS Number: 31883-16-6
Product Number: AG007I5Y(AGN-PC-01ZT4Y)
Synonyms:
MDL No:
Molecular Formula: C6H7NO3
Molecular Weight: 141.1247

Identification/Properties

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


5-Hydroxy-2-(hydroxymethyl)pyridin-4(1H)one, also known as alkylpyridoxal, is a key compound in chemical synthesis due to its unique reactivity and versatility. This compound plays a crucial role in various synthetic pathways, particularly in the pharmaceutical and agrochemical industries.One of the primary applications of 5-Hydroxy-2-(hydroxymethyl)pyridin-4(1H)one is as a versatile building block for the synthesis of pyridoxal-5'-phosphate (PLP), a biologically active form of vitamin B6. PLP is an essential coenzyme involved in numerous enzymatic reactions, making it a valuable target for chemical synthesis. 5-Hydroxy-2-(hydroxymethyl)pyridin-4(1H)one serves as a precursor in the synthesis of PLP analogs with modified functionalities, enabling the development of novel therapeutic agents and enzyme inhibitors.Additionally, 5-Hydroxy-2-(hydroxymethyl)pyridin-4(1H)one can be utilized in the preparation of heterocyclic compounds and chelating agents. Its hydroxymethyl group offers the potential for further functionalization through various chemical reactions, such as oxidation, reduction, and substitution, allowing for the synthesis of diverse molecular structures with tailored properties.Overall, 5-Hydroxy-2-(hydroxymethyl)pyridin-4(1H)one is a valuable component in chemical synthesis, facilitating the creation of complex molecules with important biological activities and industrial applications.