Cas no 1221273-58-0 (10-Chloro-1,1-diethoxydecane)

10-Chloro-1,1-diethoxydecane is a chloro-functionalized acetal compound with the molecular formula C??H??ClO?. This intermediate is characterized by its reactive chloroalkyl group and stable diethoxy acetal moiety, making it useful in organic synthesis, particularly for the preparation of aldehydes, ketones, and other functionalized derivatives. Its structure allows for selective transformations under controlled conditions, offering versatility in pharmaceutical and fine chemical applications. The compound's stability under neutral conditions facilitates handling and storage, while its reactivity under acidic or nucleophilic conditions enables efficient downstream modifications. Suitable for use in Grignard reactions, alkylations, and as a protected aldehyde precursor, it provides a balance of reactivity and stability for synthetic applications.
10-Chloro-1,1-diethoxydecane structure
10-Chloro-1,1-diethoxydecane structure
Product Name:10-Chloro-1,1-diethoxydecane
CAS No:1221273-58-0
MF:C14H29ClO2
MW:264.831864118576
CID:819940
PubChem ID:46856372
Update Time:2025-11-01

10-Chloro-1,1-diethoxydecane Chemical and Physical Properties

Names and Identifiers

    • 10-Chloro-1,1-diethoxydecane
    • DTXSID30676797
    • 10-Chloro-1,1'-diethoxydecane
    • AKOS015918197
    • DA-18153
    • 1221273-58-0
    • CBGYUTQJILAMSR-UHFFFAOYSA-N
    • SCHEMBL596548
    • MDL: MFCD16877203
    • Inchi: 1S/C14H29ClO2/c1-3-16-14(17-4-2)12-10-8-6-5-7-9-11-13-15/h14H,3-13H2,1-2H3
    • InChI Key: CBGYUTQJILAMSR-UHFFFAOYSA-N
    • SMILES: ClCCCCCCCCCC(OCC)OCC

Computed Properties

  • Exact Mass: 264.18577
  • Monoisotopic Mass: 264.186
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 0
  • Hydrogen Bond Acceptor Count: 2
  • Heavy Atom Count: 17
  • Rotatable Bond Count: 13
  • Complexity: 136
  • Covalently-Bonded Unit Count: 1
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 0
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • Topological Polar Surface Area: 18.5A^2
  • XLogP3: 5

Experimental Properties

  • Density: 0.932±0.06 g/cm3 (20 oC 760 Torr),
  • Boiling Point: 314.2±12.0 oC (760 Torr),
  • Flash Point: 64.0±14.7 oC,
  • Solubility: Almost insoluble (0.09 g/l) (25 o C),
  • PSA: 18.46

10-Chloro-1,1-diethoxydecane Pricemore >>

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Additional information on 10-Chloro-1,1-diethoxydecane

Professional Introduction to Compound with CAS No 1221273-58-0 and Product Name: 10-Chloro-1,1-diethoxydecane

The compound with the CAS number 1221273-58-0 and the product name 10-Chloro-1,1-diethoxydecane represents a significant advancement in the field of organic chemistry and pharmaceutical applications. This compound, characterized by its unique structural and functional properties, has garnered considerable attention in recent years due to its potential in various chemical synthesis pathways and its role as an intermediate in the development of novel therapeutic agents.

10-Chloro-1,1-diethoxydecane is a chlorinated ether derivative with a decane backbone, featuring two ethoxy groups at the terminal carbon atoms. This specific arrangement imparts distinct reactivity and solubility characteristics, making it a valuable building block in synthetic chemistry. The presence of the chlorine substituent enhances its utility in nucleophilic substitution reactions, while the ethoxy groups contribute to its stability and compatibility with a wide range of organic solvents.

In recent years, there has been growing interest in the applications of 10-Chloro-1,1-diethoxydecane in pharmaceutical research. Its structural features make it an attractive candidate for the synthesis of complex molecules, including drug candidates targeting various diseases. For instance, studies have shown its potential use in the preparation of bioactive lipids and signaling molecules that play crucial roles in cellular communication and metabolic regulation.

One of the most compelling aspects of 10-Chloro-1,1-diethoxydecane is its versatility in chemical transformations. Researchers have leveraged its reactivity to develop novel synthetic routes for heterocyclic compounds, which are essential components of many modern medications. The compound's ability to undergo selective functionalization allows for the creation of diverse molecular architectures, enabling the design of drugs with tailored pharmacological properties.

Recent advancements in computational chemistry have further highlighted the importance of 10-Chloro-1,1-diethoxydecane as a key intermediate. High-throughput virtual screening methods have been employed to identify new applications for this compound, particularly in the context of enzyme inhibition and receptor binding studies. These computational approaches have revealed promising leads for drug discovery programs targeting neurological disorders and inflammatory conditions.

The synthesis of 10-Chloro-1,1-diethoxydecane itself is another area where innovation has been notable. Modern synthetic methodologies have improved both the yield and purity of this compound, making it more accessible for industrial-scale applications. Catalytic processes have been refined to minimize byproduct formation, ensuring that researchers can work with high-quality starting materials for their experiments.

In addition to its pharmaceutical relevance, 10-Chloro-1,1-diethoxydecane has found utility in materials science. Its unique solubility profile allows it to serve as a solvent or co-solvent in polymerization reactions, where it can influence the morphology and mechanical properties of resulting materials. This has opened up new possibilities for developing advanced polymers with specific functionalities for applications such as coatings and adhesives.

The environmental impact of using 10-Chloro-1,1-diethoxydecane has also been a focus of recent research. Efforts have been made to develop greener synthetic routes that reduce waste and energy consumption. Additionally, studies on its biodegradability have provided insights into how such compounds can be designed to minimize ecological footprints while maintaining their chemical efficacy.

Looking ahead, the future prospects for 10-Chloro-1,1-diethoxydecane appear bright. Ongoing research continues to uncover new applications across multiple disciplines, from medicinal chemistry to materials engineering. As our understanding of molecular interactions deepens, this compound is likely to play an even more significant role in advancing scientific knowledge and technological innovation.

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