- Description
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Details
Boc-L-aspartic acid ß-9-fluorenylmethyl ester - Additional Information
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Additional Information
Catalog Number 48025 CAS 117014-32-1 M.W. 411.45 Formula C23H25NO6 IUPAC Name (2S)-4-(9H-fluoren-9-ylmethoxy)-2-[(2-methylpropan-2-yl)oxycarbonylamino]-4-oxobutanoic acid Synonym Boc-L-aspartic acid ß-9-fluorenylmethyl ester Also Known As - (2S)-4-(9H-fluoren-9-ylmethoxy)-2-[(2-methylpropan-2-yl)oxycarbonylamino]-4-oxobutanoic acid
- (2S)-2-(tert-butoxycarbonylamino)-4-(9H-fluoren-9-ylmethoxy)-4-oxo-butanoic acid
- (2S)-2-[(tert-butoxy-oxomethyl)amino]-4-(9H-fluoren-9-ylmethoxy)-4-oxobutanoic acid
- (2S)-2-(tert-butoxycarbonylamino)-4-(9H-fluoren-9-ylmethoxy)-4-keto-butyric acid
- (2S)-4-(9H-fluoren-9-ylmethoxy)-2-[(2-methylpropan-2-yl)oxycarbonylamino]-4-oxo-butanoic acid
- 117014-32-1
- N-alpha-tert-Butyloxycarbonyl-aspartic acid gamma-fluorenylmethyl ester
- Nalpha-Boc-asp-gamma-fluorenylmethyl ester
- BA-gamma-Fme
- L-Aspartic acid, N-((1,1-dimethylethoxy)carbonyl)-, 4-(9H-fluoren-9-ylmethyl) ester
InChIKey NHLRMCFWGFPSLT-IBGZPJMESA-N InChI InChI=1S/C23H25NO6/c1-23(2,3)30-22(28)24-19(21(26)27)12-20(25)29-13-18-16-10-6-4-8-14(16)15-9-5-7-11-17(15)18/h4-11,18-19H,12-13H2,1-3H3,(H,24,28)(H,26,27)/t19-/m0/s1 SMILES CC(C)(C)OC(=O)N[C@@H](CC(=O)OCC1C2=CC=CC=C2C3=CC=CC=C13)C(=O)O - Cited Uses
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Details
1. Robles J et al, "Solid-phase synthesis of a nucleopeptide from the linking site of adenovirus-2 nucleoprotein, -Ser(p5'CATCAT)-Gly-Asp-. Convergent versus stepwise strategy.", Nucleic Acids Research, 23(20) pp.4151-4161 (1995 Oct 25). - Reviews
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Peptides & Peptide Synthesis Products