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Structure of 1932145-07-7
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This trifluoromethyl-substituted pyrrolidine carbamate features a sterically hindered tert-butyl carbamate protecting group, enabling stable handling and compatibility with diverse synthetic transformations. The electron-deficient trifluoromethyl moiety enhances metabolic stability and modulates electronic properties in bioactive molecule design.
1,1-Dimethylethyl N-[(3R,4S)-4-(trifluoromethyl)-3-pyrrolidinyl]carbamate serves as a stable, bench-friendly building block for the synthesis of pyrrolidine-based pharmacophores. The tert-butyl carbamate group enables straightforward deprotection under mild acidic conditions, while the (3R,4S)-configured pyrrolidine core with a trifluoromethyl substituent provides enhanced metabolic stability and lipophilicity. This scaffold facilitates efficient incorporation into bioactive molecules via standard coupling reactions and supports orthogonal functionalization in complex molecule assembly.
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Lot numbers can be found on the outside label of a product: