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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)-

2,4-DIAMINO-6-HYDROXYPYRIMIDINE

Nc1cc(O)nc(n1)N Request for Quotation
Chemical Name: 2,4-DIAMINO-6-HYDROXYPYRIMIDINE
CAS Number: 100643-27-4
Product Number: AG0002KB(AGN-PC-0NV132)
Synonyms:
MDL No:
Molecular Formula: C4H6N4O
Molecular Weight: 126.1166

Identification/Properties

Computed Properties
Molecular Weight:
126.119g/mol
XLogP3:
-1.8
Hydrogen Bond Donor Count:
3
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
0
Exact Mass:
126.054g/mol
Monoisotopic Mass:
126.054g/mol
Topological Polar Surface Area:
93.5A^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

NMR Spectrum

Other Analytical Data

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Chemical Structure


2,6-Diaminopyrimidin-4-ol, also known as DAP, is a key building block in chemical synthesis, particularly in the pharmaceutical industry. This compound plays a crucial role in the production of various drugs and active pharmaceutical ingredients (APIs) due to its versatile reactivity and functional groups.In chemical synthesis, 2,6-Diaminopyrimidin-4-ol is commonly used as a precursor for the creation of more complex molecules. Its amino groups can participate in important reactions such as acylation, alkylation, and condensation, allowing for the formation of diverse chemical structures. Additionally, the hydroxyl group present in DAP provides an opportunity for further derivatization, enabling the introduction of additional functionalities for specific purposes.The application of 2,6-Diaminopyrimidin-4-ol in chemical synthesis extends beyond pharmaceuticals and can also be found in other industries such as agrochemicals, materials science, and biotechnology. Its ability to serve as a foundational component for the construction of various compounds underscores its significance in the realm of organic chemistry and highlights its importance in driving innovation and advancements in the field.