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CAS 37882-75-0: thieno[3,2-b]thiophene-2,5-dicarbaldehyde
Formula:C8H4O2S2
InChI:InChI=1/C8H4O2S2/c9-3-5-1-7-8(11-5)2-6(4-10)12-7/h1-4H
SMILES:c1c(C=O)sc2cc(C=O)sc12
Synonyms:- Thieno[3,2-B]Thiophene-2,5-Dicarboxaldehyde
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Thieno[3,2-b]thiophene-2,5-dicarbaldehyde
CAS:Thieno[3,2-b]thiophene-2,5-dicarbaldehydePurity:95%Molecular weight:196.25g/molThieno[3,2-b]thiophene-2,5-dicarbaldehyde
CAS:Purity:95.0%Color and Shape:SolidMolecular weight:196.24000549316406Thieno[3,2-b]thiophene-2,5-dicarboxaldehyde
CAS:Formula:C8H4O2S2Purity:97%Color and Shape:SolidMolecular weight:196.2462Thieno[3,2-b]thiophene-2,5-dicarboxaldehyde
CAS:Formula:C8H4O2S2Purity:>93.0%(GC)Color and Shape:Orange to Brown powder to crystalMolecular weight:196.24Thieno[3,2-b]thiophene-2,5-dicarboxaldehyde
CAS:Thieno[3,2-b]thiophene-2,5-dicarboxaldehyde is a novel biomimetic compound with an electron deficient heterocyclic ring. It has been shown to have optical properties that are dependent on the type of irradiation and can be used as a photocatalyst for the production of hydrogen from water. Thieno[3,2-b]thiophene-2,5-dicarboxaldehyde also has high electrocatalytic activity and is able to reduce electron deficient molecules in aqueous solutions. This compound was found to have a linear range that extends up to 20,000 nmr units and can be separated using gel permeation chromatography. Thieno[3,2-b]thiophene-2,5-dicarboxaldehyde also has high reactivity towards alkynes and alkenes and can be used as an acceptor in nanosheets with various architecturesFormula:C8H4O2S2Purity:Min. 95%Molecular weight:196.25 g/mol
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