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    67617-35-0

    Catalog No. EBD599372

    CAS 67617-35-0

    Name H-D-Leu-O-tBu

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    Basic Information

    Synonyms: H-D-Leu-O-tBu D-Leu-O-t-Bu d-Leu-OtBu H-D-Leu-OtBu.HCl D-Leucinetert·butylesterhydrochloride H-D-LEU-OTBUHCL H-D-LEU-OBUTHCL D-LEUCINET-BUTYLESTERHYDROCHLORIDESALT D-LEUCINET-BUTYLESTERHYDROCHLORIDE D-LEUCINE-OTBUHCL H-D-Leu-OtBu·HCl D-LeucineTert-ButylEsterHydrochloride tert-ButylD-leucinatehydrochloride(1:1) 2-Methyl-2-propanylD-leucinatehydrochloride(1:1)D-Leucine,1,1-dimethylethylester,hydrochloride(1:1)

    Molecular Formula: C10H21NO2

    Molecular Weight: 187.28

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

    Product Description:
    D-tert-Butyl leucinate is a chiral amino acid derivative, specifically the tert-butyl ester of D-leucine. It is a white to off-white crystalline powder. The compound features a tert-butyl ester protecting group, which is commonly used in peptide synthesis to mask the carboxylic acid functionality, and the D-configuration of the leucine side chain. This compound serves as a crucial chiral building block in the pharmaceutical industry. Its primary application is as a key intermediate in the synthesis of various peptide-based drugs and bioactive molecules. The tert-butyl ester group provides stability during synthesis and can be selectively removed under mild acidic conditions, making it a versatile synthon for constructing complex peptide sequences. The D-amino acid configuration is particularly important for creating peptides with enhanced metabolic stability or specific biological activities, such as in the development of enzyme inhibitors or receptor modulators. As a protected form of a non-natural amino acid, it is a valuable reagent in medicinal chemistry research for structure-activity relationship (SAR) studies and the production of potential therapeutic agents targeting a range of diseases.
    Physical Properties
    mg g kg ml l t