The compound "(3R,4S)-4-(3-bromophenyl)-1-tert-butoxycarbonyl-pyrrolidine-3-carboxylic acid," identified by its CAS number 959582-16-2, is a chiral pyrrolidine derivative featuring a tert-butoxycarbonyl (Boc) protecting group and a carboxylic acid functional group. Its structure includes a pyrrolidine ring, which contributes to its potential biological activity, and a bromophenyl substituent that may enhance its lipophilicity and interaction with biological targets. The presence of the Boc group indicates that this compound is likely used in synthetic organic chemistry, particularly in peptide synthesis or as an intermediate in drug development. The stereochemistry, denoted by the (3R,4S) configuration, suggests specific spatial arrangements that can influence the compound's reactivity and interaction with enzymes or receptors. Overall, this compound may exhibit interesting pharmacological properties, making it a subject of interest in medicinal chemistry and drug design.

(3R,4S)-4-(3-bromophenyl)-1-tert-butoxycarbonyl-pyrrolidine-3-carboxylic acid

959582-16-2: (3S,4R)-1-Boc-4-(3-Bromophenyl)Pyrrolidine-3-Carboxylic Acid

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CAS 959582-16-2: (3R,4S)-4-(3-bromophenyl)-1-tert-butoxycarbonyl-pyrrolidine-3-carboxylic acid

(3R,4S)-4-(3-Bromophenyl)-1-(tert-butoxycarbonyl)-pyrrolidine-3-carboxylic acid

Ref: 3D-JNB58216