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Atomfair 2,3-Dioxabicyclo[2.2.1]heptane C5H8O2
Description 2,3-Dioxabicyclo[2.2.1]heptane (CAS No. 2880-89-9) is a highly specialized bicyclic organic compound with the molecular formula C5H8O2. This heterocyclic compound features a unique bridged structure containing two oxygen atoms within its bicyclo[2.2.1]heptane framework, making it a valuable intermediate in synthetic organic chemistry and materials science. With a purity grade suitable for research applications, this product is ideal for use in the development of novel pharmaceuticals, agrochemicals, and functional materials. It is supplied as a clear, colorless to pale yellow liquid under standard conditions and should be stored in a cool, dry place away from oxidizing agents. Researchers will appreciate its…
Description
Description
2,3-Dioxabicyclo[2.2.1]heptane (CAS No. 2880-89-9) is a highly specialized bicyclic organic compound with the molecular formula C5H8O2. This heterocyclic compound features a unique bridged structure containing two oxygen atoms within its bicyclo[2.2.1]heptane framework, making it a valuable intermediate in synthetic organic chemistry and materials science. With a purity grade suitable for research applications, this product is ideal for use in the development of novel pharmaceuticals, agrochemicals, and functional materials. It is supplied as a clear, colorless to pale yellow liquid under standard conditions and should be stored in a cool, dry place away from oxidizing agents. Researchers will appreciate its well-characterized properties and potential as a building block for complex molecular architectures.
- CAS No: 2880-89-9
- Molecular Formula: C5H8O2
- Molecular Weight: 100.12
- Exact Mass: 100.052429494
- Monoisotopic Mass: 100.052429494
- IUPAC Name: 2,3-dioxabicyclo[2.2.1]heptane
- SMILES: C1CC2CC1OO2
- Synonyms: 2,3-Dioxabicyclo[2.2.1]heptane, 2,3-Dioxabicyclo(2.2.1)heptane, 279-35-6, DTXSID90950580, DTXCID301378730
Application
2,3-Dioxabicyclo[2.2.1]heptane serves as a versatile precursor in organic synthesis, particularly in the construction of oxygen-containing heterocycles and strained ring systems. Researchers utilize this compound in the development of novel pharmaceutical candidates due to its unique structural motif. It also finds application in polymer chemistry as a monomer for specialty resins with tailored thermal and mechanical properties. Additionally, its reactivity makes it suitable for studying ring-opening reactions and catalytic transformations.
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