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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(3H)-Pyrimidinone,6-(methylamino)-

CNc1cc(O)ncn1 Request for Quotation
Chemical Name: 4(3H)-Pyrimidinone,6-(methylamino)-
CAS Number: 1122-67-4
Product Number: AG00832Z(AGN-PC-0P387H)
Synonyms:
MDL No:
Molecular Formula: C5H7N3O
Molecular Weight: 125.1286

Identification/Properties

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
-
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


6-(Methylamino)pyrimidin-4-ol, also known as MAP, is a versatile compound widely used in chemical synthesis. With its unique structural properties, MAP plays a crucial role in various organic reactions and serves as a valuable building block in the creation of complex molecules.One of the key applications of 6-(Methylamino)pyrimidin-4-ol in chemical synthesis is its utility as a nucleophilic reagent. Due to the presence of the methylamino group, MAP exhibits nucleophilic behavior, making it an excellent candidate for participating in substitution and addition reactions. This reactivity allows for the selective functionalization of specific sites within a molecule, enabling chemists to tailor the synthetic route towards desired products.Additionally, 6-(Methylamino)pyrimidin-4-ol can act as a precursor for the synthesis of biologically active compounds. By incorporating MAP into the molecular structure, medicinal chemists can introduce specific functionalities or pharmacophores that enhance the biological activity or pharmacokinetic properties of the final product. This strategic use of MAP in synthetic pathways highlights its significance in drug discovery and development processes.Furthermore, the ability of 6-(Methylamino)pyrimidin-4-ol to undergo diverse transformations, such as oxidation or reduction reactions, further expands its synthetic utility. Chemists can exploit these chemical modifications to access a wide range of derivatives with varied properties and functionalities, opening up possibilities for innovation and discovery in the field of organic chemistry.In summary, 6-(Methylamino)pyrimidin-4-ol is a valuable tool in chemical synthesis, offering precise control over reactivity and enabling the construction of complex molecules with tailored properties. Its versatility and adaptability make it an indispensable component in the toolkit of synthetic chemists seeking to explore new frontiers in organic synthesis.