2-(D-Xylo-Tetrahydroxybutyl)-4(R)-1,3-Thiazolidine-4-Carboxylic Acid, with the CAS number 110270-19-4, is a chemical compound characterized by its thiazolidine ring structure, which incorporates a carboxylic acid functional group. This compound features a tetrahydroxybutyl side chain, contributing to its hydrophilicity and potential biological activity. The presence of multiple hydroxyl groups suggests that it may participate in hydrogen bonding, influencing its solubility and reactivity in aqueous environments. The thiazolidine moiety is often associated with various pharmacological properties, including potential roles in metabolic processes. The stereochemistry indicated by the (R) configuration at the thiazolidine carbon may affect its biological interactions and efficacy. Overall, this compound's unique structural features position it as a subject of interest in medicinal chemistry and biochemistry, particularly in the context of drug development and metabolic studies. Further research would be necessary to elucidate its specific applications and mechanisms of action.

2-(D-XYLO-TETRAHYDROXYBUTYL)-4(R)-1,3-THIAZOLIDINE-4-CARBOXYLIC ACID

110270-19-4: 2-(D-Xylo-Tetrahydroxybutyl)-4(R)-1,3-Thiazolidine-4-Carboxylic Acid, with the CAS number 110270-19-4, is a chemical compound characterized by its thiazolidine ring structure, which incorporates a carboxylic acid functional group. This compound features a tetrahydroxybutyl side chain, contributing to its hydrophilicity and potential biological activity. The presence of multiple hydroxyl groups suggests that it may participate in hydrogen bonding, influencing its solubility and reactivity in aqueous environments. The thiazolidine moiety is often associated with various pharmacological properties, including potential roles in metabolic processes. The stereochemistry indicated by the (R) configuration at the thiazolidine carbon may affect its biological interactions and efficacy. Overall, this compound's unique structural features position it as a subject of interest in medicinal chemistry and biochemistry, particularly in the context of drug development and metabolic studies. Further research would be necessary to elucidate its specific applications and mechanisms of action.

(2R,4R)-2-[D-Xylo-tetrahydroxybut-1-yl]-1,3-thiazolidine-4-carboxylic acid

<p>(2R,4R)-2-[D-Xylo-tetrahydroxybut-1-yl]-1,3-thiazolidine-4-carboxylic acid is a methylated saccharide that has been modified by the click chemistry method. It is a synthetic product with high purity and good quality. This compound can be used for glycosylation and oligosaccharide synthesis. (2R,4R)-2-[D-Xylo-tetrahydroxybut-1-yl]-1,3-thiazolidine-4-carboxylic acid has CAS No. 110270-19-4 and can be found in complex carbohydrates in nature.</p>

CAS 110270-19-4

2-(D-XYLO-TETRAHYDROXYBUTYL)-4(R)-1,3-THIAZOLIDINE-4-CARBOXYLIC ACID

(2R,4R)-2-[D-Xylo-tetrahydroxybut-1-yl]-1,3-thiazolidine-4-carboxylic acid

Ref: 7W-GC2335

(2R,4R)-2-[D-Xylo-tetrahydroxybut-1-yl]-1,3-thiazolidine-4-carboxylic acid

Ref: 3D-MX01042