110270-19-4

Basic information

• Product Name: 2-(D-XYLO-TETRAHYDROXYBUTYL)-4(R)-1,3-THIAZOLIDINE-4-CARBOXYLIC ACID
• Synonyms: 2-(D-XYLO-TETRAHYDROXYBUTYL)-4(R)-1,3-THIAZOLIDINE-4-CARBOXYLIC ACID;(2R,4R)-2-[D-Xylo-tetrahydroxybut-1-yl]-1,3-thiazolidine-4-carboxylicacid;2-D-Xylo-tetrahydroxybutyl-4-R-1,3-thiazolidine-4-carboxylic
• CAS NO: 110270-19-4
• Molecular Formula: C₈H₁₅NO₆S
• Molecular Weight: 253.273
• Mol File: 110270-19-4.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 654.4±55.0 °C(Predicted)
• Appearance: /
• Density: 1.624±0.06 g/cm3(Predicted)
• PKA: 1.97±0.40(Predicted)
• CAS DataBase Reference: 2-(D-XYLO-TETRAHYDROXYBUTYL)-4(R)-1,3-THIAZOLIDINE-4-CARBOXYLIC ACID(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(D-XYLO-TETRAHYDROXYBUTYL)-4(R)-1,3-THIAZOLIDINE-4-CARBOXYLIC ACID(110270-19-4)
• EPA Substance Registry System: 2-(D-XYLO-TETRAHYDROXYBUTYL)-4(R)-1,3-THIAZOLIDINE-4-CARBOXYLIC ACID(110270-19-4)

Safety Data

• Hazardous Substances Data: 110270-19-4(Hazardous Substances Data)

Usage

General Description

2-(D-xylo-tetrahydroxybutyl)-4(R)-1,3-thiazolidine-4-carboxylic acid is a chemical compound with a molecular formula of C12H21NO8S. It is a derivative of thiazolidine carboxylic acid and contains a xylose component. 2-(D-XYLO-TETRAHYDROXYBUTYL)-4(R)-1,3-THIAZOLIDINE-4-CARBOXYLIC ACID has potential biological activities and has been studied for its potential pharmaceutical applications. It is a chiral molecule, with a specific configuration at the 4th carbon and the carbon adjacent to the thiazolidine ring. Further research is needed to fully understand the properties and potential applications of this chemical compound.

Upstream product

• 5328-37-0 L-arabinose 
• 10318-18-0 DL-cysteine hydrochloride 
• 1114-34-7 D-lyxose 
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• 58-86-6 D-xylose 
• 52-90-4 L-Cysteine 

Downstream Products

• 921-01-7 D-cysteine 

Relevant articles and documents

Proton and Zinc(II) Complexes of 2-(Polyhydroxyalkyl)thiazolidine-4-carboxylic acid Derivatives

The protonation and zinc-ion co-ordination equilibria of 2-(polyhydroxyalkyl)thiazolidine-4-carboxylic acid derivatives have been studied by potentiometric titration in the range pH 1.5-8.In most cases the formation of complexes with a metal-to-ligand ratio of 1:2 was demonstrated, but at above pH 6 mixed-ligand complexes involving hydroxide-ion co-ordination were also observed.The protonation and complex-formation constants were shown to depend on the structure of the polyhydroxy chains.In the case of the protonation constants this is due to the rearrangement of the intramolecular hydrogen-bonding network, while the complex-formation constants depend on the conformation of the OH groups on the first carbon atoms of the polyol chains.

Resolution of DL-Cysteine

The diastereomeric 4-thiazolidinecarboxylic acids 3 and 4, obtained by condensation of DL-cysteine (DL-1) with D-(+)-galactose (2), can be separated by crystallization.Ring cleavage of 3 or 4 gives L-cysteine (L-1) or D-cysteine (D-1), respectively.Instead of D-(+)-galactose other chiral aldoses can be employed as resolution agents.