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2,5-Di(2-thienyl)thiophene 1081-34-1

2,5-Di(2-thienyl)thiophene 1081-34-1

Name: 2, 2', 2"-Terthiophene Other name: 2, 2': 5’, 2"-Terthiophene ; 2,5-Di(2-thienyl)thiophene ; α -Terthienyl CAS: 1081-34-1 EINECS: N/A MF: C12H8S3 MW: 248.39 MP: 93-95 °C(lit.) Appearance: pale-yellow powder Purity: 98%min. Package: 25g; 100g; 500g; 1Kg, bulk package 2,...

    Name: 2, 2', 2"-Terthiophene

    Other name: 2, 2': 5’, 2"-Terthiophene; 2,5-Di(2-thienyl)thiophene; α-Terthienyl

    CAS: 1081-34-1

    EINECS: N/A

    MF: C12H8S3

    MW: 248.39

    MP: 93-95 °C(lit.)

    Appearance: pale-yellow powder

    Purity: 98%min.

    Package: 25g; 100g; 500g; 1Kg, bulk package

     

    2, 2': 5’, 2"-Terthiophene is the organic compound with the formula [C4H3S]2C4H2S. It is an oligomer of the heterocycle thiophene, a shorter oligomer is dithienyl, and the parent polymer is polythiophene. In the most common isomer of terthiophene, two thienyl groups are connected via their 2 positions to a central thiophene, also at the carbon atoms flanking the sulfur.

    Terthiophene is prepared by the nickel- or palladium-catalysed coupling reaction of 2,5-dibromothiophene with the Grignard reagent derived from 2-bromothiophene.

    This isomer is a pigment in African marigolds (Tagetes spp.) and exhibits some biological activity because it sensitizes the formation of singlet oxygen. It is responsible for the insecticidal activity of Tagetes minuta.

    2, 2': 5’, 2"-Terthiophene has been employed as building block for the organic semi-conductor polythiophene.

    Specifications of Terthiophene.jpg

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