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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-hydrazino-

NNc1cc(O)ncn1 Request for Quotation
Chemical Name: 4(1H)-Pyrimidinone, 6-hydrazino-
CAS Number: 29939-37-5
Product Number: AG00C1ZI(AGN-PC-0KEWCU)
Synonyms:
MDL No:
Molecular Formula: C4H6N4O
Molecular Weight: 126.1166

Identification/Properties

Properties
MP:
237 °C
BP:
316°C at 760 mmHg
Storage:
Inert atmosphere;-10 ℃;
Form:
Solid
Computed Properties
Molecular Weight:
126.119g/mol
XLogP3:
-1.3
Hydrogen Bond Donor Count:
3
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
1
Exact Mass:
126.054g/mol
Monoisotopic Mass:
126.054g/mol
Topological Polar Surface Area:
79.5A^2
Heavy Atom Count:
9
Formal Charge:
0
Complexity:
183
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-6-hydrazinylpyrimidine is a versatile compound widely used in chemical synthesis for its valuable reactivity and functional groups. In organic chemistry, it serves as a key building block for the synthesis of various heterocyclic compounds due to its unique structure and properties. This compound plays a crucial role in the development of pharmaceuticals, agrochemicals, and materials science by enabling the construction of complex molecular structures through various reaction pathways. Its hydrazinyl and hydroxyl groups allow for the formation of diverse chemical bonds, making it an essential component in the creation of novel compounds with potential applications in different industries. Additionally, 4-Hydroxy-6-hydrazinylpyrimidine has been studied for its ability to participate in multiple synthetic transformations, highlighting its importance as a valuable tool in organic synthesis.