3-(R)-(tert-Butoxycarbonylamino)pyrrolidine

• CAT Number: R021689
• CAS Number: 122536-77-0
• Molecular Formula: C9H18N2O2
• Molecular Weight: 186.26
• Purity: ≥95%
• Synonyms: (3R)-3-Pyrrolidinylcarbamic Acid 1,1-Dimethylethyl Ester; (R)-3-Pyrrolidinylcarbamic Acid 1,1-Dimethylethyl Ester; (3R)-(+)-3-Bocaminopyrrolidine; (3R)-(+)-3-[(tert-Butoxycarbonyl)amino]pyrrolidine; (3R)-3-(N-tert-Butoxycarbonylamino)pyrrolidine; (3R
• Storage: -20°C
• IUPAC Name: tert-butyl N-[(3R)-pyrrolidin-3-yl]carbamate
• InChI: InChI=1S/C9H18N2O2/c1-9(2,3)13-8(12)11-7-4-5-10-6-7/h7,10H,4-6H2,1-3H3,(H,11,12)/t7-/m1/s1
• InChIKey: DQQJBEAXSOOCPG-SSDOTTSWSA-N
• SMILES: CC(C)(C)OC(=O)NC1CCNC1

3-(R)-(tert-Butoxycarbonylamino)pyrrolidine (Cat No.: R021689) is a chiral, nitrogen-containing heterocyclic compound used primarily as a protected intermediate in organic and medicinal chemistry. It features a pyrrolidine ring with an (R)-configured amino group at the 3-position, protected by a tert-butoxycarbonyl (Boc) group. The Boc group shields the amine during multistep synthesis, allowing selective reactions elsewhere in the molecule. This compound is commonly employed in the synthesis of pharmaceuticals, peptides, and fine chemicals, where stereocontrol and temporary amine protection are critical for product specificity and yield.