Date published: 2025-11-1

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Sodium thiophenolate (CAS 930-69-8)

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Alternate Names:
Benzenethiol sodium salt; Sodium thiophenoxide; Thiophenol sodium salt
Application:
Sodium thiophenolate is a reagent employed in aromatic substitution reactions
CAS Number:
930-69-8
Purity:
≥90%
Molecular Weight:
132.16
Molecular Formula:
C6H5SNa
Supplemental Information:
This is classified as a Dangerous Good for transport and may be subject to additional shipping charges.
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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Sodium thiophenolate plays a role in advancing organosulfur chemistry by serving as a versatile nucleophile in numerous organic synthesis pathways. Sodium thiophenolate is critical for crafting sulfur-containing aromatic compounds, which are key due to their significant potential in materials science and catalytic processes. It acts effectively in the formation of metal complexes by acting as a ligand, where it binds to various metals, aiding in the exploration and development of complexes noted for their unique catalytic and electronic characteristics. Sodium thiophenolate facilitates the incorporation of sulfur functionalities into polymers, thereby enhancing their conductive and mechanical features. Its utility extends to environmental chemistry, where it contributes to the mitigation of pollution by participating in the removal of heavy metals from waste streams via sophisticated precipitation and complexation mechanisms.


Sodium thiophenolate (CAS 930-69-8) References

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  2. Umpolung Difunctionalization of Carbonyls via Visible-Light Photoredox Catalytic Radical-Carbanion Relay.  |  Wang, S., et al. 2020. J Am Chem Soc. 142: 7524-7531. PMID: 32233431
  3. Temperature-Dependent Reactivity of a Non-heme FeIII(OH)(SR) Complex: Relevance to Isopenicillin N Synthase.  |  Yadav, V., et al. 2021. J Am Chem Soc. 143: 46-52. PMID: 33356198
  4. Preparation and Synthetic Application of Naproxen-Containing Diaryliodonium Salts.  |  Zhou, J., et al. 2021. Molecules. 26: PMID: 34071240
  5. New Analogs of Polyamine Toxins from Spiders and Wasps: Liquid Phase Fragment Synthesis and Evaluation of Antiproliferative Activity.  |  Vassileiou, C., et al. 2022. Molecules. 27: PMID: 35056762
  6. Field-induced reagent concentration and sulfur adsorption enable efficient electrocatalytic semihydrogenation of alkynes.  |  Gao, Y., et al. 2022. Sci Adv. 8: eabm9477. PMID: 35196082
  7. Determination of Methyl Methanesulfonate and Ethyl Methylsulfonate in New Drug for the Treatment of Fatty Liver Using Derivatization Followed by High-Performance Liquid Chromatography with Ultraviolet Detection.  |  Wang, Y., et al. 2022. Molecules. 27: PMID: 35335314
  8. Palladium-catalyzed bisthiolation of terminal alkynes for the assembly of diverse (Z)-1,2-bis(arylthio)alkene derivatives.  |  Lai, YL., et al. 2021. RSC Adv. 11: 28447-28451. PMID: 35478536
  9. Strain-Release Driven Epoxidation and Aziridination of Bicyclo[1.1.0]butanes via Palladium Catalyzed σ-Bond Nucleopalladation.  |  Wölfl, B., et al. 2023. Angew Chem Int Ed Engl. 62: e202217064. PMID: 36507714
  10. Photochemical halogen-bonding assisted generation of vinyl and sulfur-centered radicals: stereoselective catalyst-free C(sp2)-S bond forming reactions.  |  Piedra, HF. and Plaza, M. 2023. Chem Sci. 14: 650-657. PMID: 36741527
  11. Deaminative bromination, chlorination, and iodination of primary amines.  |  Xue, JH., et al. 2023. iScience. 26: 106255. PMID: 36909668
  12. Synthetic Potential of Regio- and Stereoselective Ring Expansion Reactions of Six-Membered Carbo- and Heterocyclic Ring Systems: A Review.  |  Noor, R., et al. 2023. Int J Mol Sci. 24: PMID: 37047665
  13. Reactivity of electrophilic cyclopropanes.  |  Eitzinger, A. and Ofial, AR. 2023. Pure Appl Chem. 95: 389-400. PMID: 37252340

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Sodium thiophenolate, 10 g

sc-255621
10 g
$49.00