Cas no 56187-93-0 (4-(Phenyl-D5)-3-buten-2-one)

4-(Phenyl-D5)-3-buten-2-one is a deuterated analog of 4-phenyl-3-buten-2-one, where the phenyl ring hydrogens are replaced with deuterium (D5). This isotopic labeling enhances its utility in NMR spectroscopy and mass spectrometry, providing improved signal resolution and reduced background interference in structural and mechanistic studies. The compound is particularly valuable in kinetic isotope effect (KIE) investigations and metabolic research, where deuterium substitution aids in tracing reaction pathways. Its high isotopic purity and stability make it suitable for use in pharmaceutical and biochemical applications, including drug metabolism studies and isotopic dilution analyses. The product is synthesized under controlled conditions to ensure consistent quality and performance.
4-(Phenyl-D5)-3-buten-2-one structure
4-(Phenyl-D5)-3-buten-2-one structure
Product Name:4-(Phenyl-D5)-3-buten-2-one
CAS No:56187-93-0
MF:C10H10O
MW:151.216611385345
CID:889920
PubChem ID:12224734
Update Time:2025-06-13

4-(Phenyl-D5)-3-buten-2-one Chemical and Physical Properties

Names and Identifiers

    • 4-(Phenyl-D5)-3-buten-2-one
    • 4-(Phenyl-d5)-2-butenone
    • Acetocinnamone-d5
    • Benzalacetone-d5
    • Benzylideneacetone-d5
    • Methyl 2-(Phenyl-d5)vinyl Ketone
    • Methyl Styryl Ketone-d5
    • NSC 5605-d5
    • 4-(Phenyl-d5)-3-bute
    • [2H5]benzonitrile
    • 491896_ALDRICH
    • 4-pentadeuteriophenyl-but-3-en-2-one
    • AG-E-54248
    • benzonitrile-d5
    • Benzonitrile-d5(7CI,8CI,9CI)
    • CTK8F7976
    • d5-benzonitrile
    • Penta-Deuterio-benzonitril
    • pentadeuterio-benzonitrile
    • pentadeuterobenzonitrile
    • Pentadeuterobenzyliden-aceton
    • perdeuterated cyanobenzene
    • Phenyl-d5 cyanide
    • 56187-93-0
    • (3E)-4-[(2,3,4,5,6-?H?)phenyl]but-3-en-2-one
    • (E)-4-(2,3,4,5,6-Pentadeuteriophenyl)but-3-en-2-one
    • Inchi: 1S/C10H10O/c1-9(11)7-8-10-5-3-2-4-6-10/h2-8H,1H3/b8-7+/i2D,3D,4D,5D,6D
    • InChI Key: BWHOZHOGCMHOBV-XLKVIOBLSA-N
    • SMILES: O=C(C)/C=C/C1C([2H])=C([2H])C([2H])=C([2H])C=1[2H]

Computed Properties

  • Exact Mass: 156.1359
  • Monoisotopic Mass: 151.104548668g/mol
  • Isotope Atom Count: 5
  • Hydrogen Bond Donor Count: 0
  • Hydrogen Bond Acceptor Count: 1
  • Heavy Atom Count: 11
  • Rotatable Bond Count: 2
  • Complexity: 152
  • Covalently-Bonded Unit Count: 1
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 0
  • Defined Bond Stereocenter Count: 1
  • Undefined Bond Stereocenter Count: 0
  • XLogP3: 2.1
  • Topological Polar Surface Area: 17.1?2

Experimental Properties

  • PSA: 17.07

4-(Phenyl-D5)-3-buten-2-one Pricemore >>

Related Categories No. Product Name Cas No. Purity Specification Price update time Inquiry
TRC
P319582-5mg
4-(Phenyl-d5)-3-buten-2-one
56187-93-0
5mg
$ 184.00 2023-09-06
TRC
P319582-50mg
4-(Phenyl-d5)-3-buten-2-one
56187-93-0
50mg
$ 1453.00 2023-09-06

Additional information on 4-(Phenyl-D5)-3-buten-2-one

Research Briefing on 4-(Phenyl-D5)-3-buten-2-one (CAS: 56187-93-0) in Chemical and Biomedical Applications

4-(Phenyl-D5)-3-buten-2-one (CAS: 56187-93-0) is a deuterated analog of 4-phenyl-3-buten-2-one, a compound of significant interest in chemical and biomedical research due to its versatile applications in synthetic chemistry, drug development, and metabolic studies. The incorporation of deuterium (D5) at the phenyl ring enhances its utility as a stable isotope-labeled internal standard in mass spectrometry-based assays, improving the accuracy and precision of quantitative analyses in pharmacokinetic and metabolomic studies. Recent advancements in the synthesis and application of this compound have expanded its role in cutting-edge research.

Recent studies have focused on optimizing the synthetic pathways for 4-(Phenyl-D5)-3-buten-2-one to achieve higher yields and purity, which are critical for its use in high-sensitivity analytical techniques. A 2023 publication in the Journal of Labelled Compounds and Radiopharmaceuticals detailed a novel catalytic deuteration method that minimizes side reactions and maximizes isotopic purity. This method employs palladium-based catalysts under mild conditions, offering a scalable and cost-effective approach for industrial and academic laboratories.

In the biomedical field, 4-(Phenyl-D5)-3-buten-2-one has been employed as a key intermediate in the synthesis of deuterated drug candidates. Its stable isotope labeling allows for precise tracking of drug metabolites in vivo, facilitating the development of new therapeutic agents with improved metabolic stability and reduced toxicity. A recent study in the European Journal of Medicinal Chemistry highlighted its use in the synthesis of deuterated kinase inhibitors, which demonstrated enhanced pharmacokinetic profiles in preclinical models.

Furthermore, the compound's role in elucidating metabolic pathways has been underscored by its application in isotope dilution mass spectrometry (IDMS). Researchers have utilized 4-(Phenyl-D5)-3-buten-2-one to quantify endogenous metabolites in complex biological matrices, enabling breakthroughs in understanding disease mechanisms and biomarker discovery. A 2024 study published in Analytical Chemistry reported its successful use in profiling oxidative stress markers in neurodegenerative diseases, providing new insights into disease progression and potential therapeutic targets.

In conclusion, 4-(Phenyl-D5)-3-buten-2-one (CAS: 56187-93-0) continues to be a valuable tool in chemical and biomedical research, with its applications spanning synthetic chemistry, drug development, and metabolic studies. Ongoing research efforts are expected to further expand its utility, particularly in the development of next-generation deuterated pharmaceuticals and advanced analytical methodologies. Future directions may include exploring its potential in targeted drug delivery systems and as a probe for studying enzyme mechanisms.

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