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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(1H)-Pyrimidinone, 6-hydroxy-2-methyl-

O=c1cc(O)[nH]c(n1)C Request for Quotation
Chemical Name: 4(1H)-Pyrimidinone, 6-hydroxy-2-methyl-
CAS Number: 1194-22-5
Product Number: AG000IOT(AGN-PC-0NZV05)
Synonyms:
MDL No:
Molecular Formula: C5H6N2O2
Molecular Weight: 126.1133

Identification/Properties

Computed Properties
Molecular Weight:
126.115g/mol
XLogP3:
-0.9
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
0
Exact Mass:
126.043g/mol
Monoisotopic Mass:
126.043g/mol
Topological Polar Surface Area:
61.7A^2
Heavy Atom Count:
9
Formal Charge:
0
Complexity:
205
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:
H302+H312+H332-H315-H319-H335
Precautionary Statements:
P261-P280-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


2-Methyl-4,6-dihydroxypyrimidine, also known as DHMP, is a versatile compound widely utilized in chemical synthesis for its unique properties and reactivity. In organic chemistry, DHMP serves as a key building block for the synthesis of various pharmaceuticals, agrochemicals, and functional materials.Its hydroxyl groups make it a valuable intermediate in the preparation of complex molecules, as they can undergo various chemical transformations such as esterification, etherification, and oxidation reactions. DHMP's structure provides multiple sites for functionalization, enabling the introduction of different functional groups to tailor the properties of the final product.One of the prominent applications of 2-Methyl-4,6-dihydroxypyrimidine is in the synthesis of nucleoside analogs, which are vital components in the development of antiviral and anticancer drugs. By incorporating DHMP into the nucleoside structure, researchers can enhance the bioactivity and pharmacokinetic profiles of these therapeutic agents.Furthermore, DHMP finds use in the preparation of complex heterocyclic compounds, which are essential in drug discovery and materials science. Its ability to participate in cyclization reactions allows for the construction of diverse ring systems with specific functionalities, offering new possibilities for molecular design and optimization.Overall, the versatility and reactivity of 2-Methyl-4,6-dihydroxypyrimidine make it a valuable tool in chemical synthesis, enabling the efficient and strategic construction of diverse organic molecules with potential applications in various fields.