4-​Chlorothiophenol(4-Chlorobenzenethiol)

For research use only. Not for therapeutic Use.

  • CAT Number: R017979
  • CAS Number: 106-54-7
  • Molecular Formula: C6H5ClS
  • Molecular Weight: 144.616
  • Purity: ≥95%
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<p>
<span style="color:#000000;"><span style="font-family:arial,helvetica,sans-serif;"><span style="font-size:12px;">4-​Chlorothiophenol(4-Chlorobenzenethiol) (CAS&nbsp;106-54-7)&nbsp;<span style="font-variant-ligatures: normal; orphans: 2; widows: 2;">undergoes oxidative coupling catalyzed by iron(III)-tetra phenyl prophyrin to form disulfides.&nbsp;</span><span style="font-variant-ligatures: normal; orphans: 2; widows: 2;">4-Chlorothiophenol was used to modify poly(vinyl chloride) and to synthesize poly(vinyl chloride) with halogen groups.</span></span></span></span></p>


Catalog Number R017979
CAS Number 106-54-7
Synonyms

4-Chlorobenzenethiol; p-Chlorobenzenethiol; 1-Chloro-4-mercaptobenzene; 4-Chlorobenzenethiol; 4-Chlorophenylmercaptan; 4-Chlorophenylthiol; 4-Mercaptophenyl chloride; NSC 18714; NSC 229564; p-Chlorobenzenethiol; p-Chlorophenylmercaptan; p-Chloropheny

Molecular Formula C6H5ClS
Purity ≥95%
Storage -20°C
IUPAC Name 4-chlorobenzenethiol
InChI InChI=1S/C6H5ClS/c7-5-1-3-6(8)4-2-5/h1-4,8H
InChIKey VZXOZSQDJJNBRC-UHFFFAOYSA-N
SMILES C1=CC(=CC=C1S)Cl
Reference

<p>
<span style="color:#000000;"><span style="font-family:arial,helvetica,sans-serif;"><span style="font-size:12px;">1.<span style="font-variant-ligatures: normal; orphans: 2; widows: 2;">KARIMI, BAHADOR, et al. &quot;Selective Oxidation of Thiols to Disulfides Catalyzed by Iron (III)–Tetra Phenyl Porphyrin Using Urea-Hydrogen Peroxide as Oxidizing Reagent.&quot;&nbsp;</span><i style="font-family: Arial, sans-serif; font-size: 13px; font-variant-ligatures: normal; orphans: 2; widows: 2;">Turkish Journal of Chemistry</i><span style="font-variant-ligatures: normal; orphans: 2; widows: 2;">&nbsp;29.5 (2005): 539-546.<br />
2.</span><span style="font-variant-ligatures: normal; orphans: 2; widows: 2;">Navarro, Rodrigo, et al. &quot;Modification of poly (vinyl chloride) with new aromatic thiol compounds. Synthesis and characterization.&quot;&nbsp;</span><i style="font-family: Arial, sans-serif; font-size: 13px; font-variant-ligatures: normal; orphans: 2; widows: 2;">Polymer degradation and stability</i><span style="font-variant-ligatures: normal; orphans: 2; widows: 2;">&nbsp;93.3 (2008): 585-591.</span></span></span></span></p>

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