108199-25-3

Basic information

• Product Name: 2,5-Thiophenedicarboxylic acid, 3,4-dihydroxy-, 2,5-dimethyl ester, sodium salt
• Synonyms: 2,5-Thiophenedicarboxylic acid, 3,4-dihydroxy-, 2,5-dimethyl ester, sodium salt;3,4-Dihydroxy-2,5-thiophenedicarboxylic acid dimethyl ester disodium salt;3,4-Dihydroxythiophene-2,5-dicarboxylic acid, diMethyl ester, sodiuM salt;2,5-Thiophenedicarboxylic acid, 3,4-dihydroxy-, 2,5-diMethyl ester, sodiuM salt (1:2);DiMethyl 3,4-dihydroxythiophene-2,5-dicarboxylate, disodiuM salt;3,4-Dihydroxy-2,5-thiophenedicarboxylic acid dimethyl ester diso
• CAS NO: 108199-25-3
• Molecular Formula: C8H6Na2O6S
• Molecular Weight: 254.19235
• Mol File: 108199-25-3.mol
• Article Data: 2

Chemical Properties

• Appearance: /
• Storage Temp.: Keep in dark place,Inert atmosphere,Room temperature
• CAS DataBase Reference: 2,5-Thiophenedicarboxylic acid, 3,4-dihydroxy-, 2,5-dimethyl ester, sodium salt(CAS DataBase Reference)
• NIST Chemistry Reference: 2,5-Thiophenedicarboxylic acid, 3,4-dihydroxy-, 2,5-dimethyl ester, sodium salt(108199-25-3)
• EPA Substance Registry System: 2,5-Thiophenedicarboxylic acid, 3,4-dihydroxy-, 2,5-dimethyl ester, sodium salt(108199-25-3)

Safety Data

• Hazardous Substances Data: 108199-25-3(Hazardous Substances Data)

Usage

General Description

The chemical 2,5-Thiophenedicarboxylic acid, 3,4-dihydroxy-, 2,5-dimethyl ester, sodium salt is a synthesized organic compound that is commonly used in the pharmaceutical industry as a building block for various drugs and pharmaceutical products. It is also used as a reagent in organic synthesis and as a solubilizing agent in drug formulations. This chemical is derived from thiophene, a heterocyclic compound, and has two carboxylic acid groups and two hydroxyl groups, making it a versatile compound for various chemical reactions and applications. Its sodium salt form enhances its solubility and stability, making it a preferred choice for pharmaceutical and chemical applications.

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Relevant articles and documents

Synthesis and crystal structures of 2,3,12,13-tetraalkoxy-21,23- dithiaporphyrins and 2,3-dialkoxy-21-monothiaporphyrins

The tetraalkoxy and dialkoxy substituted 21,23-dithiaporphyrins and 21-monothiaporphyrins, respectively, having methoxy, butoxy, octyloxy and dodecyloxy substituents at β-thiophene carbons were synthesized and characterized. The X-ray structure was solved for tetrabutoxy substituted 21,23-dithiaporphyrin and it exhibited a more planar structure compared with unsubstituted S2TPP, whereas the dimethoxy substituted 21-monothiaporphyrin showed a saddle shaped structure similar to unsubstituted STPPH. A series of 21,23-dithia and 21-monothiaporphyrins having methoxy, butoxy, octyloxy and dodecyloxy substituents at β-thiophene carbons were synthesized and characterized.