Cas no 119725-81-4 (3-(1,1-Dioxidotetrahydro-2H-thiopyran-3-yl)pentanedioic Acid)

3-(1,1-Dioxidotetrahydro-2H-thiopyran-3-yl)pentanedioic Acid is a sulfone-containing dicarboxylic acid derivative with potential applications in organic synthesis and pharmaceutical research. Its unique structure, featuring a tetrahydrothiopyran ring with a sulfone group and a flexible pentanedioic acid side chain, offers versatility as a building block for complex molecules. The sulfone moiety enhances stability and may influence reactivity in selective transformations, while the dicarboxylic acid functionality provides sites for further derivatization. This compound is particularly valuable for designing biologically active molecules or functional materials, where its balanced polarity and structural rigidity can be advantageous. Its synthetic utility is supported by well-defined chemical properties and compatibility with standard reaction conditions.
3-(1,1-Dioxidotetrahydro-2H-thiopyran-3-yl)pentanedioic Acid structure
119725-81-4 structure
Product Name:3-(1,1-Dioxidotetrahydro-2H-thiopyran-3-yl)pentanedioic Acid
CAS No:119725-81-4
MF:C10H16O6S
MW:264.2954
CID:5068014
Update Time:2025-05-19

3-(1,1-Dioxidotetrahydro-2H-thiopyran-3-yl)pentanedioic Acid Chemical and Physical Properties

Names and Identifiers

    • Cycloxydim-sulfone-glutaric acid
    • 3-(1,1-dioxothian-3-yl)pentanedioic acid
    • 3-(1,1-Dioxidotetrahydro-2H-thiopyran-3-yl)pentanedioic Acid
    • Inchi: 1S/C10H16O6S/c11-9(12)4-8(5-10(13)14)7-2-1-3-17(15,16)6-7/h7-8H,1-6H2,(H,11,12)(H,13,14)
    • InChI Key: ZQTHHTAJXROHTN-UHFFFAOYSA-N
    • SMILES: S1(C([H])([H])C([H])([H])C([H])([H])C([H])(C1([H])[H])C([H])(C([H])([H])C(=O)O[H])C([H])([H])C(=O)O[H])(=O)=O

Computed Properties

  • Hydrogen Bond Donor Count: 2
  • Hydrogen Bond Acceptor Count: 6
  • Heavy Atom Count: 17
  • Rotatable Bond Count: 5
  • Complexity: 378
  • XLogP3: -0.4
  • Topological Polar Surface Area: 117

3-(1,1-Dioxidotetrahydro-2H-thiopyran-3-yl)pentanedioic Acid Pricemore >>

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Additional information on 3-(1,1-Dioxidotetrahydro-2H-thiopyran-3-yl)pentanedioic Acid

3-(1,1-Dioxidotetrahydro-2H-thiopyran-3-yl)pentanedioic Acid: A Comprehensive Overview

The compound 3-(1,1-Dioxidotetrahydro-2H-thiopyran-3-yl)pentanedioic Acid (CAS No. 119725-81-4) is a unique organic molecule with significant potential in various scientific and industrial applications. This compound belongs to the class of pentanedioic acids, which are known for their versatile chemical properties and wide-ranging uses in fields such as pharmaceuticals, agrochemicals, and materials science.

Pentanedioic acid, also known as glutaric acid, is a dicarboxylic acid with two carboxylic acid groups attached to a five-carbon chain. The presence of the thiopyran ring in this compound introduces additional functional groups that enhance its reactivity and versatility. The thiopyran ring is a six-membered ring containing sulfur atoms, which can undergo various chemical transformations depending on the reaction conditions.

Recent studies have highlighted the importance of 3-(1,1-Dioxidotetrahydro-2H-thiopyran-3-yl)pentanedioic Acid in the development of advanced materials. For instance, researchers have explored its use as a precursor for synthesizing high-performance polymers and composites. The compound's ability to form strong intermolecular bonds makes it an ideal candidate for applications requiring high thermal stability and mechanical strength.

In the pharmaceutical industry, this compound has shown promise as a building block for drug delivery systems. Its unique structure allows for the creation of biocompatible materials that can encapsulate and release drugs in a controlled manner. This property is particularly valuable in the development of targeted drug delivery systems, which aim to minimize side effects and improve therapeutic outcomes.

The synthesis of 3-(1,1-Dioxidotetrahydro-2H-thiopyran-3-yl)pentanedioic Acid involves a multi-step process that combines organic synthesis techniques with advanced catalytic methods. Recent advancements in catalysis have enabled the production of this compound with higher yields and improved purity levels, making it more accessible for large-scale applications.

One of the most exciting developments in this field is the use of this compound in bio-based materials. Researchers have successfully incorporated it into biodegradable polymers that can be used in packaging, agriculture, and other industries where environmental sustainability is a priority. The compound's ability to participate in both traditional and bio-inspired reactions opens up new avenues for green chemistry.

In addition to its practical applications, 3-(1,1-Dioxidotetrahydro-2H-thiopyran-3-yl)pentanedioic Acid has also been studied for its potential role in energy storage systems. Its unique electronic properties make it a candidate for use in advanced battery technologies and supercapacitors. Ongoing research aims to optimize its performance in these applications by modifying its structure through various chemical pathways.

The compound's versatility is further demonstrated by its use in analytical chemistry as a chelating agent. Its ability to bind metal ions makes it useful in various separation techniques and sensing applications. Recent studies have explored its potential as a sensing material for heavy metal ions, which are harmful to both human health and the environment.

In conclusion, 3-(1,1-Dioxidotetrahydro-2H-thiopyran-3-yl)pentanedioic Acid (CAS No. 119725-81-4) is a multifaceted compound with significant potential across diverse fields. Its unique structure and reactivity make it an invaluable tool for scientists and engineers seeking innovative solutions to complex problems. As research continues to uncover new applications for this compound, its role in advancing technology and improving quality of life will undoubtedly grow.

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