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Atomfair Thieno(3,4-b)thiophene-2-carboxylic acid C7H4O2S2
Description Thieno[3,4-b]thiophene-2-carboxylic acid (CAS No. 14630-08-1) is a high-purity heterocyclic carboxylic acid with the molecular formula C7H4O2S2. This specialized organic compound features a fused thienothiophene core, offering unique electronic and structural properties for advanced research applications. Our product is rigorously tested to ensure ??98% purity (HPLC) and is supplied as a fine crystalline powder with excellent batch-to-batch consistency. The material is carefully packaged under inert atmosphere to maintain stability and is ideal for use in organic electronics, conjugated polymer synthesis, and as a building block for novel semiconducting materials. Each shipment includes comprehensive analytical documentation including1H NMR,13C NMR, and mass…
Description
Description
Thieno[3,4-b]thiophene-2-carboxylic acid (CAS No. 14630-08-1) is a high-purity heterocyclic carboxylic acid with the molecular formula C7H4O2S2. This specialized organic compound features a fused thienothiophene core, offering unique electronic and structural properties for advanced research applications. Our product is rigorously tested to ensure ??98% purity (HPLC) and is supplied as a fine crystalline powder with excellent batch-to-batch consistency. The material is carefully packaged under inert atmosphere to maintain stability and is ideal for use in organic electronics, conjugated polymer synthesis, and as a building block for novel semiconducting materials. Each shipment includes comprehensive analytical documentation including 1H NMR, 13C NMR, and mass spectrometry data.
- CAS No: 14630-08-1
- Molecular Formula: C7H4O2S2
- Molecular Weight: 184.2
- Exact Mass: 183.96527171
- Monoisotopic Mass: 183.96527171
- IUPAC Name: thieno[2,3-c]thiophene-2-carboxylic acid
- SMILES: C1=C(SC2=CSC=C21)C(=O)O
- Synonyms: Thieno[3,4-b]thiophene-2-carboxylic acid, 14630-08-1, Thieno(3,4-b)thiophene-2-carboxylic acid, 886-093-6, thieno[2,3-c]thiophene-2-carboxylic acid
Application
This compound serves as a key precursor in the synthesis of conjugated polymers for organic photovoltaics and field-effect transistors. Researchers utilize its carboxylic acid functionality for esterification or amidation reactions to create novel ??-conjugated systems. The thienothiophene moiety contributes to enhanced charge carrier mobility in organic electronic materials. It’s particularly valuable in developing low-bandgap polymers for solar cell applications.
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