Cas no 37021-14-0 (3-ethyl-1-phenyl-2-sulfanylideneimidazolidin-4-one)

3-Ethyl-1-phenyl-2-sulfanylideneimidazolidin-4-one is a heterocyclic compound featuring an imidazolidinone core with a phenyl substituent at the 1-position and a thione (sulfanylidene) group at the 2-position. This structure confers reactivity useful in organic synthesis, particularly as a building block for pharmaceuticals and agrochemicals. The ethyl group enhances solubility in organic solvents, while the thione moiety offers versatile reactivity for further functionalization, such as nucleophilic substitution or metal coordination. Its stable crystalline form ensures consistent handling and storage. The compound’s well-defined structure and functional groups make it valuable for applications in medicinal chemistry and material science, where precise molecular modifications are required.
3-ethyl-1-phenyl-2-sulfanylideneimidazolidin-4-one structure
37021-14-0 structure
Product Name:3-ethyl-1-phenyl-2-sulfanylideneimidazolidin-4-one
CAS No:37021-14-0
MF:C11H12N2OS
MW:220.290781021118
MDL:MFCD00541210
CID:310301
PubChem ID:169847
Update Time:2025-06-26

3-ethyl-1-phenyl-2-sulfanylideneimidazolidin-4-one Chemical and Physical Properties

Names and Identifiers

    • 4-Imidazolidinone,3-ethyl-1-phenyl-2-thioxo-
    • 3-ethyl-1-phenyl-2-sulfanylideneimidazolidin-4-one
    • 3-Ethyl-1-phenyl-2-thioxoimidazolidin-4-one
    • UYPCZQJGNPASBR-UHFFFAOYSA-N
    • SCHEMBL10383197
    • 4-Imidazolidinone, 3-ethyl-1-phenyl-2-thioxo-
    • AKOS000313236
    • 37021-14-0
    • 3-Ethyl-1-phenyl-2-thioxo-4-imidazolidinone #
    • NS00030140
    • EN300-230543
    • EINECS 253-310-5
    • CS-0298309
    • 5107-57-3
    • SR-01000389512-1
    • 3-Ethyl-1-phenyl-2-thioxo-4-imidazolidinone
    • DTXSID6068018
    • SR-01000389512
    • 3-Ethyl-1-phenyl-2-thiohydantoin
    • HMS1577P01
    • AG-690/09706020
    • STK075482
    • 3-Ethyl-1-phenyl-2-thioxo-imidazolidin-4-one
    • MDL： MFCD00541210
    • Inchi： 1S/C11H12N2OS/c1-2-12-10(14)8-13(11(12)15)9-6-4-3-5-7-9/h3-7H,2,8H2,1H3
    • InChI Key： UYPCZQJGNPASBR-UHFFFAOYSA-N
    • SMILES： S=C1N(CC)C(CN1C1C=CC=CC=1)=O

Computed Properties

  • Exact Mass: 220.06716
  • Monoisotopic Mass: 220.067034
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 0
  • Hydrogen Bond Acceptor Count: 3
  • Heavy Atom Count: 15
  • Rotatable Bond Count: 2
  • Complexity: 274
  • Covalently-Bonded Unit Count: 1
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 0
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • Topological Polar Surface Area: 55.6
  • XLogP3: 1.8

Experimental Properties

  • Density: 1.3
  • Boiling Point: 310.7°Cat760mmHg
  • Flash Point: 141.7°C
  • Refractive Index: 1.666
  • PSA: 23.55

3-ethyl-1-phenyl-2-sulfanylideneimidazolidin-4-one Pricemore >>

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Enamine
EN300-230543-0.05g
3-ethyl-1-phenyl-2-sulfanylideneimidazolidin-4-one
 37021-14-0 95%
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Enamine
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EN300-230543-1.0g
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Enamine
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3-ethyl-1-phenyl-2-sulfanylideneimidazolidin-4-one Related Literature

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Additional information on 3-ethyl-1-phenyl-2-sulfanylideneimidazolidin-4-one

Comprehensive Overview of 3-ethyl-1-phenyl-2-sulfanylideneimidazolidin-4-one (CAS No. 37021-14-0)

3-ethyl-1-phenyl-2-sulfanylideneimidazolidin-4-one (CAS No. 37021-14-0) is a specialized organic compound that has garnered significant attention in the fields of medicinal chemistry and material science. This compound, characterized by its unique imidazolidinone core and sulfanylidene functional group, is widely studied for its potential applications in drug development and industrial processes. Researchers are particularly interested in its structural versatility, which allows for modifications to enhance its biological activity or physical properties.

In recent years, the demand for 3-ethyl-1-phenyl-2-sulfanylideneimidazolidin-4-one has increased due to its relevance in pharmaceutical intermediates and organic synthesis. The compound's CAS No. 37021-14-0 is frequently searched in academic databases and chemical supplier platforms, reflecting its importance in research and development. Its phenyl and ethyl substituents contribute to its stability and reactivity, making it a valuable building block for more complex molecules.

One of the trending topics related to this compound is its potential role in green chemistry. As industries shift toward sustainable practices, 3-ethyl-1-phenyl-2-sulfanylideneimidazolidin-4-one is being explored for its compatibility with eco-friendly synthesis methods. Questions like "How can CAS No. 37021-14-0 be synthesized with minimal environmental impact?" are increasingly common in scientific forums and search engines, highlighting the intersection of chemistry and sustainability.

Another area of interest is the compound's applicability in biomedical research. Studies suggest that derivatives of 3-ethyl-1-phenyl-2-sulfanylideneimidazolidin-4-one may exhibit antimicrobial or anti-inflammatory properties, though further validation is required. Researchers often inquire about its mechanism of action and structure-activity relationships, which are critical for optimizing its therapeutic potential.

From a technical perspective, the sulfanylidene group in CAS No. 37021-14-0 offers unique reactivity patterns, enabling its use in catalysis and polymer chemistry. Its ability to participate in cross-coupling reactions and cycloadditions makes it a versatile reagent in synthetic organic chemistry. These attributes align with the growing demand for high-performance materials and specialty chemicals in advanced manufacturing.

In summary, 3-ethyl-1-phenyl-2-sulfanylideneimidazolidin-4-one (CAS No. 37021-14-0) is a compound of broad scientific and industrial relevance. Its applications span drug discovery, sustainable chemistry, and material science, making it a focal point for ongoing research. As the scientific community continues to explore its properties, this compound is poised to play a pivotal role in addressing contemporary challenges in chemistry and beyond.

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