Thiophene

For research use only. Not for therapeutic Use.

  • CAT Number: R016795
  • CAS Number: 110-02-1
  • Molecular Formula: C4H4S
  • Molecular Weight: 84.136
  • Purity: ≥95%
Inquiry Now

<span style="color:#000000;"><span style="font-family:arial,helvetica,sans-serif;"><span style="font-size:12px;">Thiophene (CAS&nbsp;110-02-1)&nbsp;is an essential precursor to synthesize a wide range of conjugated organosulfur moieties, sulfur-containing polycyclic aromatic hydrocarbons, macrocycles, and pharmaceutical compounds.It has been widely used in the synthesis of polythiophenes and a host of active materials for organic field effect transistors (OFETs) and organic solar cells (OSCs).</span></span></span>


Catalog Number R016795
CAS Number 110-02-1
Synonyms

CP 34; Divinylene sulfide; Furan, thio-; Huile H50; Huile HSO; NSC 405073; Thiacyclopentadiene; Thiaphene; Thiofuran; Thiofurfuran; Thiole; Thiophen; Thiotetrole;

Molecular Formula C4H4S
Purity ≥95%
Storage -20°C
IUPAC Name thiophene
InChI InChI=1S/C4H4S/c1-2-4-5-3-1/h1-4H
InChIKey YTPLMLYBLZKORZ-UHFFFAOYSA-N
SMILES C1=CSC=C1
Reference

<span style="font-family:arial,helvetica,sans-serif;"><span style="font-size:12px;">1.Bianchini, Claudio, and Andrea Meli. &quot;Thiophene, Benzo [b] thiophene and Dibenzo [b, d] thiophene as Precursors to Highly Conjugated Organosulfur Compounds.&quot;&nbsp;<i style="font-family: Arial, sans-serif; font-size: 13px;">Synlett</i>&nbsp;1997.06 (1997): 643-649.<br />
2.Hu, Peng, et al. &quot;Palladium‐Catalyzed Decarboxylative C-H Bond Arylation of Thiophenes.&quot;&nbsp;<i style="font-family: Arial, sans-serif; font-size: 13px;">Angewandte Chemie</i>&nbsp;124.1 (2012): 231-235.<br />
3.Newkome, George R., et al. &quot;Construction of synthetic macrocyclic compounds possessing subheterocyclic rings, specifically pyridine, furan, and thiophene.&quot;&nbsp;<i style="font-family: Arial, sans-serif; font-size: 13px;">Chemical Reviews</i>&nbsp;77.4 (1977): 513-597.<br />
4.Ong, Beng S., et al. &quot;Thiophene Polymer Semiconductors for Organic Thin‐Film Transistors.&quot;&nbsp;<i style="font-family: Arial, sans-serif; font-size: 13px;">Chemistry&ndash;A European Journal</i>&nbsp;14.16 (2008): 4766-4778.<br />
5.Malytskyi, Volodymyr, et al. &quot;Thiophene-based push&ndash;pull chromophores for small molecule organic solar cells (SMOSCs).&quot;&nbsp;<i style="font-family: Arial, sans-serif; font-size: 13px;">RSC Advances</i>&nbsp;5.1 (2015): 354-397.<br />
6.Zhou, Jiaoyan, et al. &quot;Solution-processed and high-performance organic solar cells using small molecules with a benzodithiophene unit.&quot;&nbsp;<i style="font-family: Arial, sans-serif; font-size: 13px;">Journal of the American Chemical Society</i>&nbsp;135.23 (2013): 8484-8487.</span></span>

Request a Quote