- Description
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Details
6-amino-2-[(2-methylpropan-2-yl)oxycarbonylamino]hexanoic acid - Additional Information
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Additional Information
Catalog Number 48068 CAS 13734-28-6 M.W. 246.30 Formula C11H22N2O4 IUPAC Name 6-amino-2-[(2-methylpropan-2-yl)oxycarbonylamino]hexanoic acid Synonym No Also Known As - 6-amino-2-[(2-methylpropan-2-yl)oxycarbonylamino]hexanoic acid
- 6-amino-2-(tert-butoxycarbonylamino)hexanoic acid
- 6-amino-2-[(tert-butoxy-oxomethyl)amino]hexanoic acid
- 13734-28-6
- N2-((1,1-Dimethylethoxy)carbonyl)-L-lysine
- N-.alpha.-Boc-L-lysine
- NSC343721
- N-.alpha.-t-Boc-L-lysine
- EINECS 237-303-4
InChIKey DQUHYEDEGRNAFO-UHFFFAOYSA-N InChI InChI=1S/C11H22N2O4/c1-11(2,3)17-10(16)13-8(9(14)15)6-4-5-7-12/h8H,4-7,12H2,1-3H3,(H,13,16)(H,14,15) SMILES CC(C)(C)OC(=O)NC(CCCCN)C(=O)O - Cited Uses
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Details
1. Zeglis BM et al, "Building Blocks for the Construction of Bioorthogonally Reactive Peptides via Solid-Phase Peptide Synthesis", ChemistryOpen, 3(2) pp.48-53 (2014 Apr).2. Sahu B et al, "Synthesis of Conformationally Preorganized and Cell-Permeable Guanidine-Based ?-Peptide Nucleic Acids (?GPNAs)", The Journal of organic chemistry, 74(4) pp.1509-1516 (2009 Feb 20).3. Carl PL et al, "Protease-activated prodrugs for cancer chemotherapy", Proceedings of the National Academy of Sciences of the United States of America, 77(4) pp.2224-2228 (1980 Apr). - Reviews
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Peptides & Peptide Synthesis Products