CAS 115184-30-0

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

Description:

2-(L-Xylo-Tetrahydroxybutyl)-4(R)-1,3-Thiazolidine-4-Carboxylic Acid, with the CAS number 115184-30-0, 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 enhances its solubility in water and may influence its interaction with biological systems. The thiazolidine moiety is known for its role in various biochemical pathways, particularly in the context of amino acid metabolism and potential therapeutic applications. Additionally, the stereochemistry indicated by the (R) configuration suggests specific spatial arrangements that can affect the compound's reactivity and interaction with enzymes or receptors. Overall, this compound may exhibit interesting pharmacological properties, making it a subject of interest in medicinal chemistry and biochemistry research.

Synonyms:

• (2R,4R)-2-[L-Xylo-tetrahydroxybut-1-yl]-1,3-thiazolidine-4-carboxylicacid

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

CAS: 115184-30-0

Ref: 7W-GC3975

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

CAS: 115184-30-0

(2R,4R)-2-[L-Xylo-tetrahydroxybut-1-yl]-1,3-thiazolidine-4-carboxylic acid is a methylated saccharide that can be used for the synthesis of glycosides and other carbohydrate derivatives. (2R,4R)-2-[L-Xylo-tetrahydroxybut-1-yl]-1,3-thiazolidine-4-carboxylic acid has been shown to react with various reagents such as iodine and bromine. This product has been synthesized by Click modification.

Formula: C₈H₁₅NO₆S

Purity: Min. 95%

Molecular weight: 253.27 g/mol

Ref: 3D-MX01046