CAS 72678-92-3: 2-(3,4-dimethoxyphenyl)-1,3-thiazolidine-4-carboxylic acid

Description: 2-(3,4-Dimethoxyphenyl)-1,3-thiazolidine-4-carboxylic acid is a chemical compound characterized by its thiazolidine ring structure, which incorporates a carboxylic acid functional group and a substituted phenyl group. The presence of the 3,4-dimethoxyphenyl moiety contributes to its potential biological activity, as methoxy groups can influence the compound's solubility and reactivity. This compound is typically studied for its pharmacological properties, particularly in the context of medicinal chemistry, where thiazolidine derivatives are known for their diverse biological activities, including anti-inflammatory and antioxidant effects. The thiazolidine ring also plays a crucial role in the compound's stereochemistry, which can affect its interaction with biological targets. Additionally, the carboxylic acid group may enhance its solubility in polar solvents, making it suitable for various applications in drug formulation and development. Overall, this compound exemplifies the intersection of organic synthesis and pharmacology, highlighting the importance of structural modifications in enhancing biological efficacy.

Formula: C₁₂H₁₅NO₄S

InChI: InChI=1/C12H15NO4S/c1-16-9-4-3-7(5-10(9)17-2)11-13-8(6-18-11)12(14)15/h3-5,8,11,13H,6H2,1-2H3,(H,14,15)

Synonyms:

• 4-Thiazolidinecarboxylic acid, 2-(3,4-dimethoxyphenyl)-

2-(3,4-Dimethoxyphenyl)-1,3-thiazolidine-4-carboxylic acid

CAS: 72678-92-3

• Purity: 95.0%
• Color and Shape: Solid
• Molecular weight: 269.32000732421875

2-(3,4-Dimethoxyphenyl)-1,3-thiazolidine-4-carboxylic acid

CAS: 72678-92-3

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• Formula: C₁₂H₁₅NO₄S
• Purity: Min. 95%
• Color and Shape: Powder
• Molecular weight: 269.32 g/mol