BOC-(2S,3S)-3-Hydroxypyrrolidine-2-carboxylic acid, with the CAS number 187039-57-2, is a chemical compound characterized by its pyrrolidine ring structure, which is a five-membered cyclic amine. The "BOC" (tert-butyloxycarbonyl) group indicates that it is a protected amino acid, commonly used in peptide synthesis to temporarily shield the amine group from reactions. The compound features a hydroxyl group (-OH) at the 3-position and a carboxylic acid group (-COOH) at the 2-position, contributing to its potential as a chiral building block in organic synthesis and pharmaceutical applications. Its stereochemistry, denoted by (2S,3S), indicates specific spatial arrangements of its atoms, which can significantly influence its biological activity and interactions. The compound is typically used in research settings, particularly in the development of biologically active molecules and in the study of amino acid derivatives. As with many chemical substances, proper handling and safety precautions are essential due to potential reactivity and toxicity.

BOC-(2S,3S)-3-HYDROXYPYRROLIDINE-2-CARBOXYLIC ACID

187039-57-2: Boc-Trans-3-Hydroxy-L-Proline, Boc-(2S,3S)-3-Hydroxy-2-Pyrrolidinecarboxylic Acid, (2S,3S)-1-(Tert-Butoxycarbonyl)-3-Hydroxypyrrolidine-2-Carboxylic Acid

Please enquire for more information about Boc-trans-3-hydroxy-l-proline including the price, delivery time and more detailed product information at the technical inquiry form on this page

CAS 187039-57-2: BOC-(2S,3S)-3-HYDROXYPYRROLIDINE-2-CARBOXYLIC ACID

Boc-trans-3-hydroxy-l-proline

Ref: 3D-FB46788

(2S,3S)-1-(tert-Butoxycarbonyl)-3-hydroxypyrrolidine-2-carboxylic acid

Ref: 10-F218341

(2S,3S)-1-[(tert-butoxy)carbonyl]-3-hydroxypyrrolidine-2-carboxylic acid

Ref: IN-DA007S5N