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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-Imidazolidinone, 3-phenyl-2-thioxo-

O=C1CNC(=S)N1c1ccccc1 Request for Quotation
Chemical Name: 4-Imidazolidinone, 3-phenyl-2-thioxo-
CAS Number: 2010-15-3
Product Number: AG002D57(AGN-PC-0JV4VB)
Synonyms:
MDL No:
Molecular Formula: C9H8N2OS
Molecular Weight: 192.2376

Identification/Properties

Properties
MP:
approximate 257℃
Storage:
2-8℃;Keep in dry area;
Form:
Solid
Computed Properties
Molecular Weight:
192.236g/mol
XLogP3:
1.4
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
1
Exact Mass:
192.036g/mol
Monoisotopic Mass:
192.036g/mol
Topological Polar Surface Area:
64.4A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
236
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:
Danger
UN#:
2811
Hazard Statements:
H301
Precautionary Statements:
P501-P270-P264-P301+P310+P330-P405
Class:
6.1
Packing Group:
Ⅲ

NMR Spectrum

Other Analytical Data

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Chemical Structure


3-Phenyl-2-thioxoimidazolidin-4-one holds a vital role in chemical synthesis as a versatile building block. This compound is widely utilized in the pharmaceutical and agrochemical industries for its unique structural properties and reactivity. Its sulfur-containing heterocyclic ring provides a valuable site for various chemical reactions, allowing for the synthesis of diverse organic compounds. In organic synthesis, 3-Phenyl-2-thioxoimidazolidin-4-one is commonly employed as a key intermediate in the preparation of sulfur-containing heterocycles, which are important in drug discovery and development. It serves as a precursor for the synthesis of various biologically active molecules, such as antibiotics, antiviral agents, and anticancer drugs.Furthermore, this compound is utilized in the construction of complex organic frameworks through its participation in multicomponent reactions and cascade reactions. Its ability to act as a nucleophile or electrophile enables the formation of carbon-sulfur and carbon-nitrogen bonds, which are essential for creating structurally diverse compounds with potential pharmacological activities. Overall, the strategic incorporation of 3-Phenyl-2-thioxoimidazolidin-4-one in chemical synthesis processes contributes significantly to the development of novel compounds with promising applications in the fields of medicine and agriculture.