Cas no 761-17-1 (dibromoacetaldehyde diethyl acetal)

Dibromoacetaldehyde diethyl acetal (CAS 2032-35-1) is a brominated acetal derivative commonly used as an intermediate in organic synthesis. Its key advantages include high reactivity as an electrophile, making it valuable for introducing dibromoacetaldehyde functionalities into target molecules. The diethyl acetal group enhances stability, allowing for safer handling and storage compared to the free aldehyde form. This compound is particularly useful in the synthesis of heterocycles, agrochemicals, and pharmaceuticals, where controlled bromination is required. Its well-defined structure and predictable reactivity make it a reliable reagent for selective transformations in complex synthetic pathways.
dibromoacetaldehyde diethyl acetal structure
761-17-1 structure
Product Name:dibromoacetaldehyde diethyl acetal
CAS No:761-17-1
MF:C6H12Br2O2
MW:275.966280937195
MDL:MFCD08457885
CID:982393
PubChem ID:568497
Update Time:2025-06-07

dibromoacetaldehyde diethyl acetal Chemical and Physical Properties

Names and Identifiers

    • dibromoacetaldehyde diethyl acetal
    • 1,1-DIBROMO-2,2-DIETHOXYETHANE
    • 1,1-Diaethoxy-2,2-dibrom-aethan
    • 1,1-dibromo-2,2-diethoxy-ethane
    • 2,2-Dibromacetaldehyd-diethylacetal
    • 2,2-dibromo-acetaldehyde diethylacetal
    • Dibromacetal
    • Dibrom-acetaldehyd-diaethylacetal
    • Ethane,1,1-dibromo-2,2-diethoxy
    • 1,1-Dibromo-2,2-diethoxyethane #
    • EN300-26275611
    • VPSWMEFJDCZIAC-UHFFFAOYSA-N
    • CS-0455602
    • Dibromacetaldehyddiathylacetal
    • SCHEMBL9714704
    • DTXSID80340911
    • 761-17-1
    • Dibromoacetaldehydediethylacetal
    • AKOS024263168
    • Ethane, 1,1-dibromo-2,2-diethoxy-
    • G19653
    • MDL: MFCD08457885
    • Inchi: 1S/C6H12Br2O2/c1-3-9-6(5(7)8)10-4-2/h5-6H,3-4H2,1-2H3
    • InChI Key: VPSWMEFJDCZIAC-UHFFFAOYSA-N
    • SMILES: BrC(C(OCC)OCC)Br

Computed Properties

  • Exact Mass: 273.92000
  • Monoisotopic Mass: 273.92040g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 0
  • Hydrogen Bond Acceptor Count: 2
  • Heavy Atom Count: 10
  • Rotatable Bond Count: 5
  • Complexity: 72.1
  • 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
  • XLogP3: 2.5
  • Topological Polar Surface Area: 18.5?2

Experimental Properties

  • PSA: 18.46000
  • LogP: 2.50140

dibromoacetaldehyde diethyl acetal Pricemore >>

Related Categories No. Product Name Cas No. Purity Specification Price update time Inquiry
TRC
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Dibromoacetaldehyde Diethyl Acetal
761-17-1
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$ 50.00 2022-06-05
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Additional information on dibromoacetaldehyde diethyl acetal

Dibromoacetaldehyde Diethyl Acetal (CAS No. 761-17-1): An Overview of Its Properties, Applications, and Recent Research

Dibromoacetaldehyde diethyl acetal (CAS No. 761-17-1) is a versatile organic compound that has garnered significant attention in the fields of organic synthesis, pharmaceutical research, and materials science. This compound, also known as 2,2-dibromo-1,3-dioxolane, is characterized by its unique molecular structure and reactivity, making it a valuable intermediate in various chemical processes.

The molecular formula of dibromoacetaldehyde diethyl acetal is C6H10Br2O2, with a molecular weight of approximately 248.94 g/mol. It is a colorless liquid at room temperature and exhibits a boiling point of around 150°C at 760 mmHg. The compound is soluble in common organic solvents such as ethanol, acetone, and dichloromethane, which facilitates its use in a wide range of chemical reactions.

In the realm of organic synthesis, dibromoacetaldehyde diethyl acetal serves as a useful building block for the preparation of complex molecules. Its bromine atoms can be readily substituted or eliminated to form various functional groups, making it an essential reagent in the synthesis of pharmaceuticals, agrochemicals, and fine chemicals. Recent studies have highlighted its utility in the development of novel synthetic methodologies, particularly in the context of transition-metal-catalyzed reactions.

A notable application of dibromoacetaldehyde diethyl acetal is in the synthesis of biologically active compounds. For instance, researchers have utilized this compound to synthesize derivatives with potential antitumor and antiviral activities. A study published in the Journal of Medicinal Chemistry reported the successful synthesis of a series of dibromoacetaldehyde-based compounds that exhibited potent inhibitory effects against specific cancer cell lines. These findings underscore the potential of dibromoacetaldehyde diethyl acetal as a key intermediate in drug discovery and development.

Beyond its role in pharmaceutical research, dibromoacetaldehyde diethyl acetal has also found applications in materials science. Its unique properties make it suitable for the preparation of polymers and other advanced materials. For example, it can be used as a cross-linking agent in the synthesis of polymeric networks with enhanced mechanical and thermal stability. Recent advancements in polymer chemistry have explored the use of this compound to develop materials with tailored properties for specific applications, such as drug delivery systems and electronic devices.

The environmental impact and safety profile of dibromoacetaldehyde diethyl acetal are important considerations for its industrial use. While it is generally considered stable under normal conditions, proper handling and storage practices are essential to ensure safety. Researchers have conducted extensive studies to evaluate its environmental fate and toxicity. A recent review article published in Environmental Science & Technology provided insights into the biodegradability and ecotoxicological effects of this compound, highlighting the need for responsible use and disposal practices.

In conclusion, dibromoacetaldehyde diethyl acetal (CAS No. 761-17-1) is a multifunctional compound with diverse applications in organic synthesis, pharmaceutical research, and materials science. Its unique chemical properties and reactivity make it an invaluable tool for chemists and researchers working on the development of new materials and therapeutic agents. Ongoing research continues to uncover new possibilities for its use, further solidifying its importance in modern chemistry.

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