- Description
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Details
Nα-Fmoc-O-tert-butyl-L-threonine - Additional Information
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Additional Information
Catalog Number 41016 CAS 71989-35-0 M.W. 397.46 Formula C23H27NO5 IUPAC Name (2S,3R)-2-(9H-fluoren-9-ylmethoxycarbonylamino)-3-[(2-methylpropan-2-yl)oxy]butanoic acid Synonym Nα-Fmoc-O-tert-butyl-L-threonine Also Known As - (2S,3R)-2-(9H-fluoren-9-ylmethoxycarbonylamino)-3-[(2-methylpropan-2-yl)oxy]butanoic acid
- (2S,3R)-3-tert-butoxy-2-(9H-fluoren-9-ylmethoxycarbonylamino)butanoic acid
- (2S,3R)-3-tert-butoxy-2-[(9H-fluoren-9-ylmethoxy-oxomethyl)amino]butanoic acid
- (2S,3R)-3-tert-butoxy-2-(9H-fluoren-9-ylmethoxycarbonylamino)butyric acid
- 535184_ALDRICH
- 47622_FLUKA
- Fmoc-O-tert-butyl-L-threonine
- Fmoc-Thr(tBu)-OH
- ST5307353
- N-Fmoc-O-tert-Butyl-L-threonine
InChIKey LZOLWEQBVPVDPR-VLIAUNLRSA-N InChI InChI=1S/C23H27NO5/c1-14(29-23(2,3)4)20(21(25)26)24-22(27)28-13-19-17-11-7-5-9-15(17)16-10-6-8-12-18(16)19/h5-12,14,19-20H,13H2,1-4H3,(H,24,27)(H,25,26)/t14-,20+/m1/s1 SMILES C[C@H]([C@@H](C(=O)O)NC(=O)OCC1C2=CC=CC=C2C3=CC=CC=C13)OC(C)(C)C - Cited Uses
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Details
1. Bahta M et al, "Oxime-based linker libraries as a general approach for the rapid generation and screening of multidentate inhibitors", Nature protocols, 7(4) pp.686-702 ().2. Mahto SK et al, "A Reversible Protection Strategy to Improve Fmoc-SPPS of Peptide Thioesters by the N-Acylurea Approach", Chembiochem : a European journal of chemical biology, 12(16) pp.2488-2494 (2011 Nov 4). - Reviews
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Peptides & Peptide Synthesis Products