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    tert-Butyl 2,6-diazaspiro[3.3]heptane-2-carboxylate is a Boc-protected diazaspirocyclic amine used as a versatile building block in medicinal chemistry and organic synthesis.
    Chemical structure of tert-Butyl 2,6-diazaspiro[3,3]heptane-2-carboxylate , CAS 1041026-70-3, AChemBlock A-874

    tert-Butyl 2,6-diazaspiro[3,3]heptane-2-carboxylate

    Catalog ID: A-874

    Product Name: tert-Butyl 2,6-diazaspiro[3,3]heptane-2-carboxylate
    CAS: 1041026-70-3
    MDL: MFCD11226963
    Purity: 95%
    Appearance: white to grey solid
    FW: 198.27
    Formula: C₁₀H₁₈N₂O₂
    Smiles: CC(C)(C)OC(=O)N1CC2(CNC2)C1
    tert-Butyl 2,6-diazaspiro[3,3]heptane-2-carboxylate 95%, CAS#: 1041026-70-3, Cat ID: A-874, BUILDING BLOCKS, AChemBlock
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    update on 07-31-2026

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    Safety Information
    Safety Information
    Pictograms GHS07
    Signal Word Warning
    Hazard Statements Causes skin irritation
    Causes serious eye irritation
    May cause respiratory irritation
    Precautionary Statements Avoid breathing dust/fume/gas/mist/vapours/spray.
    Product Information
    Product Information
    Product Information
    Purity 95%
    Appearances white to grey solid
    Storage Store at -20 °C
    Shipping Room Temp
    MSDS Download MSDS
    IUPAC Name tert-butyl 2,6-diazaspiro[3.3]heptane-2-carboxylate
    HTS Code 2933998290
    Smiles CC(C)(C)OC(=O)N1CC2(CNC2)C1
    InChiKey KVOUHLVOTMOJBS-UHFFFAOYSA-N
    Product Description tert-Butyl 2,6-diazaspiro[3.3]heptane-2-carboxylate is a nitrogen-containing spirocyclic building block featuring a compact 2,6- diazaspiro[3.3]heptane core. One nitrogen is protected by a tert-butoxycarbonyl group, while the second nitrogen remains available for selective functionalization. This compound can be used in the synthesis of substituted spirocyclic amines, heterocyclic intermediates, and research compounds. Its rigid, three-dimensional scaffold makes it useful for medicinal chemistry, compound-library development, and the preparation of structurally diverse analogs.
    Product Application Used as a Boc-protected spirocyclic building block in medicinal chemistry and organic synthesis. It is suitable for preparing substituted diazaspiro compounds, heterocyclic intermediates, compound libraries, and structurally diverse research molecules.
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