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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, 3-(3,5-dichlorophenyl)-

Clc1cc(Cl)cc(c1)N1C(=O)CNC1=O Request for Quotation
Chemical Name: 2,4-Imidazolidinedione, 3-(3,5-dichlorophenyl)-
CAS Number: 27387-87-7
Product Number: AG01FNZD(AGN-PC-0JPQGZ)
Synonyms:
MDL No:
Molecular Formula: C9H6Cl2N2O2
Molecular Weight: 245.06214

Identification/Properties

Computed Properties
Molecular Weight:
245.059g/mol
XLogP3:
2.1
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
1
Exact Mass:
243.981g/mol
Monoisotopic Mass:
243.981g/mol
Topological Polar Surface Area:
49.4A^2
Heavy Atom Count:
15
Formal Charge:
0
Complexity:
288
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


3-(3,5-Dichlorophenyl)-2,4-imidazolidinedione is a versatile chemical compound frequently employed in chemical synthesis processes. This particular compound serves as a crucial building block in the creation of various pharmaceuticals, agrochemicals, and specialty chemicals. Its unique molecular structure allows for specific modifications and transformations, making it a valuable tool for organic chemists in designing and producing complex molecules of interest. Additionally, 3-(3,5-Dichlorophenyl)-2,4-imidazolidinedione demonstrates excellent reactivity and selectivity, enabling precise control over chemical reactions, thus facilitating the synthesis of intricate organic frameworks with high efficiency and purity. Its broad applicability and reliability make it a sought-after reagent in the realm of chemical synthesis, enabling the efficient production of diverse compounds with diverse functionalities and applications.