2,2′:5′,2′′-Terthiophene
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. 2,2′:5′,2′′-Terthiophene (3T) is a tri-thiophene based low band conductive polymer that is prepared by reacting 2,5-dibromothiophene and thienylmagnesium bromide in the presence of nickel catalyst.
Catalog Number | CBB1115027 |
Alternative Name(s) | 2,5-Di(2-thienyl)thiophene; α-Terthienyl |
Molecular Formula | C12H8S3 |
CAS# | 1081-34-1 |
Purity | >99% |
Inchi | 1S/C12H8S3/c1-3-9(13-7-1)11-5-6-12(15-11)10-4-2-8-14-10/h1-8H |
Inchi Key | KXSFECAJUBPPFE-UHFFFAOYSA-N |
SMILES | c1csc(c1)-c2ccc(s2)-c3cccs3 |
Size | Inquiry |
Supplier Page | https://www.amerigoscientific.com/2252-terthiophene-item-115027.html |