17087-37-5

Basic information

• Product Name: (1R)-1-C-(4-carboxy-1,3-thiazolidin-2-yl)-D-arabinitol
• Synonyms: (1R)-1-C-(4-Carboxy-1,3-thiazolidin-2-yl)-D-arabinitol; 241-148-8
• CAS NO: 17087-37-5
• Molecular Formula: C₉H₁₇NO₇S
• Molecular Weight: 283.2988
• EINECS: 241-148-8
• Mol File: 17087-37-5.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 731.5°C at 760 mmHg
• Flash Point: 396.2°C
• Density: 1.663g/cm³
• Vapor Pressure: 1.05E-24mmHg at 25°C
• Refractive Index: 1.65
• CAS DataBase Reference: (1R)-1-C-(4-carboxy-1,3-thiazolidin-2-yl)-D-arabinitol(CAS DataBase Reference)
• NIST Chemistry Reference: (1R)-1-C-(4-carboxy-1,3-thiazolidin-2-yl)-D-arabinitol(17087-37-5)
• EPA Substance Registry System: (1R)-1-C-(4-carboxy-1,3-thiazolidin-2-yl)-D-arabinitol(17087-37-5)

Safety Data

• Hazardous Substances Data: 17087-37-5(Hazardous Substances Data)

Usage

Description

(1R)-1-C-(4-carboxy-1,3-thiazolidin-2-yl)-D-arabinitol is a unique chemical compound that belongs to the class of carboxylic acids and derivatives. It is characterized by its thiazolidine structure, which incorporates both a carboxylic acid and a sugar moiety. (1R)-1-C-(4-carboxy-1,3-thiazolidin-2-yl)-D-arabinitol has garnered interest due to its potential therapeutic properties, such as its ability to inhibit specific enzymes and modulate cellular processes. Research is ongoing to explore its potential applications in treating various diseases, particularly diabetes and metabolic disorders. Further studies are necessary to fully elucidate the pharmacological profile and practical uses of (1R)-1-C-(4-carboxy-1,3-thiazolidin-2-yl)-D-arabinitol.

Uses

Used in Pharmaceutical Industry:
(1R)-1-C-(4-carboxy-1,3-thiazolidin-2-yl)-D-arabinitol is used as a potential therapeutic agent for the treatment of diabetes and metabolic disorders. Its ability to inhibit certain enzymes and modulate cellular processes makes it a candidate for further research and development in this field.
Used in Enzyme Inhibition Research:
In the field of biochemistry, (1R)-1-C-(4-carboxy-1,3-thiazolidin-2-yl)-D-arabinitol is utilized for studying enzyme inhibition. Its structure allows it to interact with specific enzymes, providing insights into enzyme function and potential therapeutic targets.
Used in Cellular Process Modulation:
(1R)-1-C-(4-carboxy-1,3-thiazolidin-2-yl)-D-arabinitol is also used in cellular biology to investigate its effects on cellular processes. Understanding how this compound influences cellular mechanisms could lead to the development of new treatments for various diseases.

Upstream product

• 3458-28-4 D-Mannose 
• 52-89-1 l-cysteine hydrochloride 
• 52-90-4 L-Cysteine 

Downstream Products

• 921-01-7 D-cysteine 
• 52-90-4 L-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.