5-ethyl-5-phenyl-2-[(1R)-1-phenylpropyl]-1,3-diazinane-4,6-dione


Chemical Name: 5-ethyl-5-phenyl-2-[(1R)-1-phenylpropyl]-1,3-diazinane-4,6-dione
CAS Number: 1189504-46-8
Product Number: AG008VV2(AGN-PC-05J38X)
Synonyms:
MDL No:
Molecular Formula: C21H24N2O2
Molecular Weight: 336.42746

Identification/Properties


Computed Properties
Molecular Weight:
336.435g/mol
XLogP3:
4
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
5
Exact Mass:
336.184g/mol
Monoisotopic Mass:
336.184g/mol
Topological Polar Surface Area:
58.2A^2
Heavy Atom Count:
25
Formal Charge:
0
Complexity:
460
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
1
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

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Chemical Structure



5-Ethyl-5-phenyl-2-(1-phenylpropyl)dihydropyrimidine-4,6(1H,5H)-dione (Mixture of Diastereomers) is a versatile compound widely used in chemical synthesis. This compound serves as a key intermediate in the synthesis of various pharmaceuticals, agrochemicals, and fine chemicals. Its unique structure makes it a valuable building block for the development of complex organic molecules.In chemical synthesis, this compound can be utilized as a nucleophilic reagent for the construction of heterocyclic compounds. Its dihydropyrimidine core provides a solid foundation for the introduction of diverse functional groups, allowing for the creation of diverse molecular architectures. Additionally, the presence of the ethyl and phenyl substituents imparts steric and electronic properties that can influence the reactivity and selectivity of subsequent chemical transformations.Moreover, the presence of the chiral centers in this compound, leading to a mixture of diastereomers, opens up opportunities for stereochemical control in synthetic pathways. By judiciously manipulating the stereochemistry of the dihydropyrimidine scaffold, chemists can access enantiopure compounds with specific biological activities or physical properties.Overall, the application of 5-Ethyl-5-phenyl-2-(1-phenylpropyl)dihydropyrimidine-4,6(1H,5H)-dione in chemical synthesis enables the efficient construction of structurally diverse molecules with potential applications across various industries. Its strategic incorporation into synthetic routes highlights its significance as a valuable tool for the creation of new and innovative chemical entities.