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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-Pyrimidinyloxy,5-nitro-

[O-][N+](=O)c1cncnc1O Request for Quotation
Chemical Name: 4-Pyrimidinyloxy,5-nitro-
CAS Number: 219543-69-8
Product Number: AG007OR5(AGN-PC-0QYFI1)
Synonyms:
MDL No:
Molecular Formula: C4H3N3O3
Molecular Weight: 141.0849

Identification/Properties

Computed Properties
Molecular Weight:
141.086g/mol
XLogP3:
-0.7
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
0
Exact Mass:
141.017g/mol
Monoisotopic Mass:
141.017g/mol
Topological Polar Surface Area:
87.3A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
237
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


4-Hydroxy-5-nitropyrimidine, also known as HNP, is a versatile compound widely used in chemical synthesis for its unique properties and reactivity. In organic chemistry, this compound serves as a valuable building block for the synthesis of various important molecules and pharmaceuticals. One key application of 4-Hydroxy-5-nitropyrimidine is as a precursor in the synthesis of biologically active compounds such as pharmaceutical drugs. Its functional groups and molecular structure make it a valuable starting material for the creation of new chemical entities with potential therapeutic benefits. Additionally, 4-Hydroxy-5-nitropyrimidine can be utilized in the development of agrochemicals, dyes, and other specialty chemicals. Its ability to undergo various chemical transformations, including nucleophilic substitutions and metal-catalyzed reactions, makes it a versatile tool for organic chemists seeking to create complex molecules.Overall, 4-Hydroxy-5-nitropyrimidine plays a crucial role in chemical synthesis by enabling the efficient construction of diverse molecules with unique properties and applications in the fields of pharmaceuticals, materials science, and agrochemicals.