108199-25-3 Usage
Uses
Used in Pharmaceutical Industry:
2,5-Thiophenedicarboxylic acid, 3,4-dihydroxy-, 2,5-dimethyl ester, sodium salt is used as a building block for the development of various drugs and pharmaceutical products. Its unique chemical structure allows it to be incorporated into a wide range of therapeutic agents, enhancing their efficacy and safety.
Used in Organic Synthesis:
2,5-Thiophenedicarboxylic acid, 3,4-dihydroxy-, 2,5-dimethyl ester, sodium salt serves as a reagent in organic synthesis, enabling the creation of new chemical entities and facilitating various chemical reactions. Its presence can improve the yield and selectivity of reactions, making it a valuable tool in the synthesis of complex organic molecules.
Used as a Solubilizing Agent in Drug Formulations:
2,5-Thiophenedicarboxylic acid, 3,4-dihydroxy-, 2,5-dimethyl ester, sodium salt is used to improve the solubility of drugs in formulations, ensuring optimal bioavailability and therapeutic efficacy. Its sodium salt form enhances its solubility, making it an ideal choice for solubilizing agents in pharmaceutical formulations.
Check Digit Verification of cas no
The CAS Registry Mumber 108199-25-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,8,1,9 and 9 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 108199-25:
(8*1)+(7*0)+(6*8)+(5*1)+(4*9)+(3*9)+(2*2)+(1*5)=133
133 % 10 = 3
So 108199-25-3 is a valid CAS Registry Number.
108199-25-3Relevant academic research and scientific papers
Synthesis and crystal structures of 2,3,12,13-tetraalkoxy-21,23- dithiaporphyrins and 2,3-dialkoxy-21-monothiaporphyrins
Agarwal, Neeraj,Hung,Ravikanth, Mangalampalli
, p. 10671 - 10680 (2007/10/03)
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.
Esters of Thiodiglycollic and Thiodipropionic Acids and 2,5-Dicarboxy-3,4-dihydroxythiophene as Potential Slow Acting Anticancer Agents
Kumar, Anil,Tilak, B. D.
, p. 880 - 882 (2007/10/02)
A series of esters of thiodiglycollic and thiodipropionic acids and 2,5-dicarboxy-3,4-dihydroxythiophene have been synthesised with a view to testing their anticancer properties.The esters, as against parent acids are expected to have a prolonged effect.
