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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)-

(6-amino-2-methylpyrimidin-4-yl)methanol

OCc1cc(N)nc(n1)C Request for Quotation
Chemical Name: (6-amino-2-methylpyrimidin-4-yl)methanol
CAS Number: 1365993-18-5
Product Number: AG001250(AGN-PC-0H3NS8)
Synonyms:
MDL No:
Molecular Formula: C6H9N3O
Molecular Weight: 139.1552

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


(6-Amino-2-methylpyrimidin-4-yl)methanol, often referred to as $name$, serves as a versatile building block in chemical synthesis. This compound is widely recognized for its pivotal role in the creation of pharmaceuticals, agrochemicals, and specialty chemicals due to its unique structural properties.In chemical synthesis, $name$ acts as a crucial intermediate in the production of various biologically active compounds. Its amino and hydroxyl groups make it an essential component for forming diverse molecular structures through processes such as condensation reactions, esterifications, and nucleophilic substitutions.Moreover, the presence of the pyrimidine ring in $name$ confers specific reactivity patterns that allow for the incorporation of this molecule into complex heterocyclic frameworks. This characteristic makes it particularly valuable in drug discovery and development, where the construction of novel molecular scaffolds is paramount.Furthermore, the methyl substituent on the pyrimidine ring enhances the lipophilicity and stability of $name$, making it suitable for applications that require interactions with biological membranes or prolonged half-lives in biological systems.In summary, the application of (6-Amino-2-methylpyrimidin-4-yl)methanol in chemical synthesis offers a wide range of opportunities for designing and synthesizing biologically active molecules with tailored properties for various industrial and pharmaceutical applications.