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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, 5-methoxy-, hydrazone

COc1c[nH]cnc1=NN Request for Quotation
Chemical Name: 4(1H)-Pyrimidinone, 5-methoxy-, hydrazone
CAS Number: 99419-06-4
Product Number: AG005SDB(AGN-PC-0OP594)
Synonyms:
MDL No:
Molecular Formula: C5H8N4O
Molecular Weight: 140.1432

Identification/Properties

Properties
MP:
184-185℃
Storage:
Inert atmosphere;-10 ℃;
Form:
Solid
Computed Properties
Molecular Weight:
140.146g/mol
XLogP3:
-0.3
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
2
Exact Mass:
140.07g/mol
Monoisotopic Mass:
140.07g/mol
Topological Polar Surface Area:
73.1A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
99.6
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

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

NMR Spectrum

Other Analytical Data

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Chemical Structure


4-Hydrazono-5-methoxy-1,4-dihydropyrimidine is a versatile compound widely utilized in chemical synthesis for its unique properties and reactivity. In organic chemistry, this compound serves as a key intermediate in the synthesis of various heterocyclic compounds, pharmaceuticals, and agrochemicals. Its hydrazone functional group allows for the formation of stable complexes with transition metals, enabling it to act as a ligand in coordination chemistry. Additionally, the presence of the dihydropyrimidine moiety provides a scaffold for further derivatization, making it a valuable building block in the preparation of diverse molecular structures. The application of 4-Hydrazono-5-methoxy-1,4-dihydropyrimidine in chemical synthesis extends to the creation of novel materials, catalysts, and biologically active compounds, highlighting its significance in advancing modern organic chemistry methodologies.