2,2′:5′,2′′-Terthiophene (TTh) may be prepared by nickel catalysed coupling reaction of grignard′s reagent derived from 2-bromothiophene and magnesium.It generates singlet oxygen. In nature, it is found in the floral extract of Tagetes minuta and Echinops grijisii. It is known to be toxic to mosquitoes.It also exihibits antifungal activity.Electrochemical copolymerization of carbazole and TTh in sodium perchlorate/acetonitrile was reported.Electrochromic copolymer based on TTh and 3, 4-ethylenedioxythiophene has been reported. TTh acts as a monomer precursor for polythiophene and as a dopant for polycarbonate.It may function as a photosensitizer.
Specifications and Purity: 10mM in DMSO
Molecular Formula: C12H8S3
Molecular Weight: 248.39
PubChem CID: 65067
Isomeric SMILES: C1=CSC(=C1)C2=CC=C(S2)C3=CC=CS3
Beilstein Registry Number: 178604
- UPC:
- 51111805
- Condition:
- New
- HazmatClass:
- No
- WeightUOM:
- LB
- MPN:
- T420542-1ml
- CAS:
- 1081-34-1
- Product Size:
- 1ml
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