BOC-4-Hydroxy-L-pyrrolidine lactone, identified by its CAS number 113775-22-7, is a chemical compound characterized by its lactone structure derived from pyrrolidine. It features a tert-butyloxycarbonyl (BOC) protecting group, which is commonly used in organic synthesis to protect amines during chemical reactions. The compound is typically a white to off-white solid and is soluble in organic solvents such as dichloromethane and dimethyl sulfoxide (DMSO). Its molecular structure includes a pyrrolidine ring with a hydroxyl group at the 4-position, contributing to its reactivity and potential applications in medicinal chemistry, particularly in the synthesis of pharmaceuticals. The BOC group can be removed under acidic conditions, allowing for the regeneration of the free amine. This compound is often utilized in peptide synthesis and other organic transformations, making it valuable in the development of biologically active molecules. As with many chemical substances, proper handling and safety precautions should be observed due to potential hazards associated with its use.

BOC-4-HYDROXY-L-PYRROLIDINE LACTONE

113775-22-7: N-T-Boc-4-Hydroxy-L-Pyrrolidine Lactone, tert-butyl (1S,4S)-3-oxo-2-oxa-5-azabicyclo[2.2.1]heptane-5-carboxylate

N-t-BOC-4-Hydroxy-L-Pyrrolidine Lactone

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CAS 113775-22-7: BOC-4-HYDROXY-L-PYRROLIDINE LACTONE

N-t-BOC-4-Hydroxy-L-Pyrrolidine Lactone

Ref: 54-OR316002

N-tert-BOC-4-hydroxy-L-pyrrolidine lactone

Ref: 3D-FB59786

2-Oxa-5-azabicyclo[2.2.1]heptane-5-carboxylic acid, 3-oxo-, 1,1-dimethylethyl ester, (1S,4S)-

Ref: IN-DA0009NN

(1S,4S)-tert-Butyl 3-oxo-2-oxa-5-azabicyclo[2.2.1]heptane-5-carboxylate

Ref: 10-F210831