tert-Butoxycarbonyl-D-proline

• CAT Number: R061046
• CAS Number: 37784-17-1
• Molecular Formula: C10H17NO4
• Molecular Weight: 215.25
• Purity: ≥95%
• Synonyms: (2R)-1,2-Pyrrolidinedicarboxylic acid 1-(1,1-dimethylethyl) ester; ?(R)-1,2-Pyrrolidinedicarboxylic acid, 1-(1,1-dimethylethyl) ester; (2R)-1-tert-Butoxycarbonylpyrrolidine-2-carboxylic acid; (R)-1-(tert-Butyloxycarbonyl)pyrrolidine-2-carboxylic acid
• Storage: -20°C
• IUPAC Name: (2R)-1-[(2-methylpropan-2-yl)oxycarbonyl]pyrrolidine-2-carboxylic acid
• InChI: InChI=1S/C10H17NO4/c1-10(2,3)15-9(14)11-6-4-5-7(11)8(12)13/h7H,4-6H2,1-3H3,(H,12,13)/t7-/m1/s1
• InChIKey: ZQEBQGAAWMOMAI-SSDOTTSWSA-N
• SMILES: CC(C)(C)OC(=O)N1CCC[C@@H]1C(=O)O

tert-Butoxycarbonyl-D-proline (Cat No.:R061046) is a protected form of the D-enantiomer of the cyclic amino acid proline, with the molecular formula C10H17NO4. The tert-butoxycarbonyl (Boc) group protects the amine functionality, making it stable under a variety of synthetic conditions and ideal for peptide synthesis. This compound appears as a white to off-white crystalline solid and is commonly used in asymmetric synthesis, chiral auxiliaries, and pharmaceutical research. The D-configuration introduces stereochemical control in peptide and small-molecule design, while the Boc group enables selective deprotection under mild acidic conditions for multi-step organic transformations.