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    1000933-99-2

    Catalog No. EBD2043592

    CAS 1000933-99-2

    Name tert-butyl 6-hydroxyspiro[3.3]heptan-2-ylcarbamate

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    Basic Information

    Synonyms: tert-butylN-(2-hydroxyspiro[3.3]heptan-6-yl)carbamate tert-Butyl(6-hydroxyspiro[3.3]heptan-2-yl)carbamate 2-(Boc-aMino)-6-hydroxysp... (6-Hydroxyspiro[3.3]hept-2-yl)carbamicacidtert-butylester tert-butyl6-hydroxyspiro[3.3]hept-2-ylcarbamate 2-(BOC-AMINO)-6-HYDROXYSPIRO[3.3]HEPTANE tert-butylN-{6-hydroxyspiro[3.3]heptan-2-yl}carbamate tert-butyl6-hydroxyspiro[3.3]heptan-2-ylcarbamate

    Molecular Formula: C12H21NO3

    Molecular Weight: 227.3

    Categories: Medicinal Chemistry > Pharmaceutical Intermediates > Drug Synthesis Building Blocks Synthetic Chemistry > Organic Building Blocks > Amines

    Product Description:
    Tert-Butyl 6-hydroxyspiro[3.3]heptan-2-ylcarbamate is a specialized organic compound featuring a spiro[3.3]heptane core structure, which is a rigid, three-dimensional bicyclic scaffold. This molecule contains both a protected amine group (as a Boc-carbamate) and a free hydroxyl group, making it a versatile bifunctional building block. This compound is primarily utilized in medicinal chemistry and drug discovery as a key intermediate for constructing novel bioactive molecules. The spiro[3.3]heptane moiety is valued for its ability to modulate the physicochemical and pharmacokinetic properties of drug candidates, such as improving solubility, metabolic stability, and membrane permeability. It serves as a crucial synthetic precursor in the development of potential therapeutic agents, particularly in programs targeting central nervous system (CNS) disorders and other areas where three-dimensional molecular frameworks are advantageous. As a protected amino alcohol derivative, it is a valuable chiral synthon for the synthesis of complex molecules. Its applications are highly specific to advanced pharmaceutical research rather than general-purpose synthesis.
    Physical Properties
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