CAS 58416-04-9: 2,5-Thiophenedicarboxylic acid, 3,4-dihydroxy-, dimethyl ester
Formula:C8H8O6S
InChI:InChI=1/C8H8O6S/c1-13-7(11)5-3(9)4(10)6(15-5)8(12)14-2/h9-10H,1-2H3
SMILES:COC(=O)c1c(c(c(C(=O)OC)s1)O)O
Synonyms:- Dimethyl 3,4-dihydroxythiophene-2,5-dicarboxylate
- 3,4-Dihydroxy-2,5-dicarboxythiophene dimethyl ester
- 3,4-Dihydroxy-thiophene-2,5-dicarboxylic acid dimethyl ester
- 3,4-Dihydroxythiophene-2,5-dicarboxylic acid diethyl ester
- (2E,5E)-2,5-bis[hydroxy(methoxy)methylidene]thiophene-3,4(2H,5H)-dione
- 3,4-Dihydroxy-thiophene-2,5-dicarboxylicaciddimethyl ester
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Found 5 products.
Dimethyl 3,4-Dihydroxy-2,5-thiophenedicarboxylate
CAS:Formula:C8H8O6SPurity:>98.0%(GC)Color and Shape:White to Almost white powder to crystalMolecular weight:232.21Dimethyl 3,4-dihydroxythiophene-2,5-dicarboxylate
CAS:Formula:C8H8O6SPurity:98%Color and Shape:SolidMolecular weight:232.2105Dimethyl 3,4-Dihydroxy-2,5-thiophenedicarboxylate
CAS:Dimethyl 3,4-dihydroxy-2,5-thiophenedicarboxylate is an organic compound with the chemical formula CH3COOCH=CHCOOH. It is a white solid that has been used as a raw material in the production of other chemicals. Dimethyl 3,4-dihydroxy-2,5-thiophenedicarboxylate can be produced from benzoic acid and methanol via tetrathiafulvalene catalysis. The yield of this compound is high and it has been shown to have favorable selectivity for the desired product over byproducts. Dimethyl 3,4-dihydroxy-2,5-thiophenedicarboxylate is also a precursor for the synthesis of dimethyl 2,6-diisopropylbenzoate. This compound reacts with ammonia at high temperatures to form methyl 2,6-diisopFormula:C8H8O6SPurity:Min. 95%Molecular weight:232.21 g/molDimethyl 3,4-dihydroxythiophene-2,5-dicarboxylate
CAS:Dimethyl 3,4-dihydroxythiophene-2,5-dicarboxylatePurity:98+%Molecular weight:232.21g/mol
