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Diphenyl sulfone (CAS 127-63-9)

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Alternate Names:
Phenyl sulfone
CAS Number:
127-63-9
Purity:
≥99%
Molecular Weight:
218.27
Molecular Formula:
C12H10O2S
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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Diphenyl sulfone (DPS) is a versatile organic compound with a myriad of applications across scientific research and industrial production. Its unique structure grants it a diverse range of properties that find utility in various fields. In scientific research, Diphenyl sulfone serves as a valuable reagent in organic synthesis and a catalyst in chemical reactions. Moreover, it plays a pivotal role as a stabilizer, ensuring their potency and effectiveness. Diphenyl sulfone′s applications extend beyond that, as it also contributes to the production of polymers, as well as acts as a stabilizer for paints, coatings, and inks. One of the essential characteristics of Diphenyl sulfone is its Lewis acid property, allowing it to accept electrons from other molecules. This aspect renders it an efficient catalyst in organic reactions, facilitating the formation of new chemical bonds. Additionally, Diphenyl sulfone can act as a nucleophile, generously donating electrons to other molecules. This capability proves especially valuable in the synthesis of complex molecules, promoting the creation of vital bonds in intricate chemical structures. Diphenyl sulfone′s adaptability and diverse range of applications make it an indispensable component in scientific research, industrial processes, and medical breakthroughs. Its ability to act as both a Lewis acid and a nucleophile positions it as a multifunctional ally in advancing various fields of study and applications.


Diphenyl sulfone (CAS 127-63-9) References

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  2. Studies on organic mercurials. XVI. On the mechanism of aromatic mercuration and the mercuration of diphenyl sulfone.  |  UKAI, T., et al. 1955. Pharm Bull. 3: 105-8. PMID: 14394812
  3. A new streptomycete producing diphenyl sulfone antibiotic--S. sulfonensis.  |  Ellaiah, P., et al. 1998. Hindustan Antibiot Bull. 40: 31-7. PMID: 16961203
  4. Heterocyclic bismuth carboxylates based on a diphenyl sulfone scaffold: synthesis and antifungal activity against Saccharomyces cerevisiae.  |  Murafuji, T., et al. 2013. Eur J Med Chem. 63: 531-5. PMID: 23535321
  5. Synthesis of substituted diphenyl sulfones and their structure-activity relationship with the antagonism of 5-НТ6 receptors.  |  Ivachtchenko, A., et al. 2013. Bioorg Med Chem. 21: 4614-27. PMID: 23787290
  6. Activity of antifungal organobismuth(III) compounds derived from alkyl aryl ketones against S. cerevisiae: comparison with a heterocyclic bismuth scaffold consisting of a diphenyl sulfone.  |  Murafuji, T., et al. 2014. Molecules. 19: 11077-95. PMID: 25076143
  7. Case of acquired cutis laxa with preceding urticarial eruption treated by diphenyl sulfone.  |  Takenaka, Y., et al. 2018. J Dermatol. 45: e292-e293. PMID: 29782046
  8. Untargeted approach for the evaluation of anthropic impact on the sheltered marine area of Portofino (Italy).  |  Di Carro, M., et al. 2018. Mar Pollut Bull. 131: 87-94. PMID: 29887008
  9. Determination of perillaldehyde in perilla herbs using relative molar sensitivity to single-reference diphenyl sulfone.  |  Masumoto, N., et al. 2019. J Nat Med. 73: 566-576. PMID: 31016636
  10. Selective and efficient catalytic and photocatalytic oxidation of diphenyl sulphide to sulfoxide and sulfone: the role of hydrogen peroxide and TiO2 polymorph.  |  Mikrut, P., et al. 2022. RSC Adv. 12: 1862-1870. PMID: 35425200
  11. The Kinetics of Formation of Microporous Polytriazine in Diphenyl Sulfone.  |  Galukhin, A., et al. 2022. Molecules. 27: PMID: 35684538
  12. Influence of fabrication method on the biological properties of modified PEEK.  |  Wei, X., et al. 2023. Dent Mater J. 42: 72-78. PMID: 36351597
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Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Diphenyl sulfone, 100 g

sc-239801
100 g
$27.00