Tert-butyl N-[(3S)-2,6-dioxotetrahydropyran-3-yl]carbamate, with the CAS number 2420-13-5, is a chemical compound characterized by its carbamate functional group and a tetrahydropyran ring structure. This compound typically exhibits properties associated with both polar and nonpolar characteristics due to the presence of the tert-butyl group, which enhances its lipophilicity, and the carbamate moiety, which can engage in hydrogen bonding. It is often utilized in organic synthesis and medicinal chemistry, particularly in the development of pharmaceuticals, due to its potential as a protecting group or intermediate in various reactions. The stereochemistry indicated by the (3S) designation suggests that the compound has specific spatial arrangements that can influence its reactivity and biological activity. Additionally, the presence of the dioxo functional groups contributes to its reactivity, making it a versatile compound in synthetic applications. As with many organic compounds, its stability and reactivity can be influenced by environmental factors such as temperature and pH.

tert-butyl N-[(3S)-2,6-dioxotetrahydropyran-3-yl]carbamate

2420-13-5: tert-Butyl [(3S)-2,6-dioxotetrahydro-2H-pyran-3-yl]carbamate

(S)-3-N-Boc-Amino-dihydro-pyran-2,6-dione

(S)-tert-Butyl (2,6-dioxotetrahydro-2H-pyran-3-yl)carbamate

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CAS 2420-13-5: tert-butyl N-[(3S)-2,6-dioxotetrahydropyran-3-yl]carbamate

(S)-3-N-Boc-Amino-dihydro-pyran-2,6-dione

Ref: 10-F040757

(S)-tert-Butyl (2,6-dioxotetrahydro-2H-pyran-3-yl)carbamate

Ref: IN-DA007O3E

(S)-3-N-Boc-Amino-dihydro-pyran-2,6-dione

Ref: 3D-CAA42013