(2R,5S)-1-(tert-Butoxycarbonyl)-5-phenylpyrrolidine-2-carboxylic acid

95%

Reagent Code: #36504
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CAS Number 158706-46-8

science Other reagents with same CAS 158706-46-8

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Weight 291.3422 g/mol
Formula C₁₆H₂₁NO₄
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MDL Number MFCD01321009
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description Product Description

This compound is primarily used in the synthesis of pharmaceutical intermediates, particularly in the development of chiral molecules. Its structure, featuring a tert-butoxycarbonyl (Boc) protecting group and a phenylpyrrolidine core, makes it valuable in peptide chemistry and drug design. It serves as a building block for creating complex molecules, especially in the production of protease inhibitors and other bioactive compounds. The Boc group allows for selective deprotection during multi-step reactions, enabling precise modifications. Its chiral nature also aids in the development of enantiomerically pure drugs, enhancing their efficacy and reducing side effects.

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inventory 100mg
10-20 days ฿7,659.00

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(2R,5S)-1-(tert-Butoxycarbonyl)-5-phenylpyrrolidine-2-carboxylic acid
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This compound is primarily used in the synthesis of pharmaceutical intermediates, particularly in the development of chiral molecules. Its structure, featuring a tert-butoxycarbonyl (Boc) protecting group and a phenylpyrrolidine core, makes it valuable in peptide chemistry and drug design. It serves as a building block for creating complex molecules, especially in the production of protease inhibitors and other bioactive compounds. The Boc group allows for selective deprotection during multi-step reactio

This compound is primarily used in the synthesis of pharmaceutical intermediates, particularly in the development of chiral molecules. Its structure, featuring a tert-butoxycarbonyl (Boc) protecting group and a phenylpyrrolidine core, makes it valuable in peptide chemistry and drug design. It serves as a building block for creating complex molecules, especially in the production of protease inhibitors and other bioactive compounds. The Boc group allows for selective deprotection during multi-step reactions, enabling precise modifications. Its chiral nature also aids in the development of enantiomerically pure drugs, enhancing their efficacy and reducing side effects.

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