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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-Imidazolidinedione, 5-(phenylmethyl)-

O=C1NC(=O)NC1Cc1ccccc1 Request for Quotation
Chemical Name: 2,4-Imidazolidinedione, 5-(phenylmethyl)-
CAS Number: 3530-82-3
Product Number: AG00I70B(AGN-PC-09RBLU)
Synonyms:
MDL No:
Molecular Formula: C10H10N2O2
Molecular Weight: 190.1986

Identification/Properties

Properties
MP:
188-189°C
Storage:
-10 ℃;
Form:
Solid
Computed Properties
Molecular Weight:
190.202g/mol
XLogP3:
0.6
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
2
Exact Mass:
190.074g/mol
Monoisotopic Mass:
190.074g/mol
Topological Polar Surface Area:
58.2A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
247
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

Safety Information

GHS Pictogram:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


5-Benzylimidazolidine-2,4-dione, also known as benzimidazolidin-2,4-dione or PZQ, is a versatile compound widely used in chemical synthesis. This white crystalline solid exhibits interesting properties that make it a valuable tool in organic chemistry. Its unique structure contains both an imidazolidine ring and a benzyl group, providing various opportunities for functionalization and reactivity.In chemical synthesis, 5-Benzylimidazolidine-2,4-dione serves as a valuable building block for the construction of complex molecules. Its imidazolidine ring can act as a versatile scaffold for constructing diverse heterocyclic compounds through modification of its functional groups. The benzyl group attached to the ring offers a handle for further derivatization, allowing for the introduction of various functional groups to tailor the compound's properties for specific applications.One common application of 5-Benzylimidazolidine-2,4-dione is as a precursor in the synthesis of biologically active molecules. By utilizing its reactivity and functional groups, chemists can introduce specific structural motifs necessary for biological activity, such as pharmacophores in drug design. Additionally, its presence in the molecular structure can improve the compound's solubility, stability, or binding affinity to biological targets.Furthermore, 5-Benzylimidazolidine-2,4-dione can be employed in the preparation of chiral compounds. Its chiral center offers opportunities for enantioselective synthesis, enabling the production of enantiopure molecules crucial in the pharmaceutical and agrochemical industries. Through appropriate manipulation of its stereochemistry, chemists can access a wide range of optically pure compounds with tailored properties.Overall, the versatility and unique reactivity of 5-Benzylimidazolidine-2,4-dione make it a valuable asset in chemical synthesis, enabling the construction of complex molecules, design of biologically active compounds, and production of enantiopure chiral molecules for various applications in organic chemistry and beyond.