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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, 1-bromo-3-chloro-5,5-dimethyl-

ClN1C(=O)N(C(C1=O)(C)C)Br Request for Quotation
Chemical Name: 2,4-Imidazolidinedione, 1-bromo-3-chloro-5,5-dimethyl-
CAS Number: 16079-88-2
Product Number: AG001VCR(AGN-PC-0JL4OX)
Synonyms:
MDL No:
Molecular Formula: C5H6BrClN2O2
Molecular Weight: 241.4703

Identification/Properties

Properties
MP:
159-163 °C
BP:
232.7°C at 760 mmHg
Storage:
Keep in dry area;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
241.469g/mol
XLogP3:
1.3
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
0
Exact Mass:
239.93g/mol
Monoisotopic Mass:
239.93g/mol
Topological Polar Surface Area:
40.6A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
231
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-H332-H335
Precautionary Statements:
P280-P305+P351+P338-P310
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


1-Bromo-3-chloro-5,5-dimethylimidazolidine-2,4-dione, a versatile chemical compound, finds widespread applications in chemical synthesis processes. Its unique molecular structure plays a crucial role in various reactions and transformations within the realm of organic chemistry.This compound is particularly valuable in the field of medicinal chemistry, where it serves as a key building block in the synthesis of pharmaceutical agents and novel drug candidates. Its reactive nature allows for the introduction of specific functional groups, enabling chemists to fine-tune the properties of synthesized compounds for targeted therapeutic purposes.Furthermore, 1-Bromo-3-chloro-5,5-dimethylimidazolidine-2,4-dione is employed in the synthesis of complex organic molecules, such as heterocycles and natural products. Its ability to participate in diverse chemical reactions, including nucleophilic substitutions and cyclization processes, makes it an indispensable tool for organic chemists seeking to access structurally intricate compounds.Moreover, this compound exhibits promising potential in material science, where it can be utilized for the preparation of advanced materials with tailored properties. By incorporating 1-Bromo-3-chloro-5,5-dimethylimidazolidine-2,4-dione into polymerization reactions or functionalization strategies, researchers can develop innovative materials with enhanced performance characteristics.In summary, the versatility of 1-Bromo-3-chloro-5,5-dimethylimidazolidine-2,4-dione in chemical synthesis makes it a valuable asset for researchers and practitioners across various disciplines, driving innovation and progress in the synthesis of biologically active compounds, complex molecules, and advanced materials.