CAS 130674-54-3
:Fmoc-D-allo-Thr-OH
Description:
Fmoc-D-allo-Thr-OH, with the CAS number 130674-54-3, is a protected amino acid commonly used in peptide synthesis. It features a phenylmethoxycarbonyl (Fmoc) group, which serves as a protective group for the amino functionality, allowing for selective reactions during peptide assembly. The "D-allo-Thr" designation indicates that it is a D-enantiomer of allo-threonine, a non-standard amino acid that differs from threonine in its side chain configuration. This compound is typically utilized in solid-phase peptide synthesis, where the Fmoc group can be easily removed under basic conditions, facilitating the sequential addition of amino acids. Fmoc-D-allo-Thr-OH is characterized by its stability under standard laboratory conditions, solubility in organic solvents, and compatibility with various coupling reagents. Its unique structure and properties make it valuable in the development of peptides with specific biological activities, particularly in research and pharmaceutical applications.
Formula:CHNO5
InChI:InChI=1S/C19H19NO5/c1-11(21)17(18(22)23)20-19(24)25-10-16-14-8-4-2-6-12(14)13-7-3-5-9-15(13)16/h2-9,11,16-17,21H,10H2,1H3,(H,20,24)(H,22,23)/t11-,17-/m1/s1
InChI key:OYULCCKKLJPNPU-PIGZYNQJSA-N
SMILES:C[C@H]([C@H](C(=O)O)NC(=O)OCC1C2=CC=CC=C2C3=CC=CC=C13)O
Synonyms:- N-alpha-(9-Fluorenylmethyloxycarbonyl)-allo-D-threonine
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Fmoc-D-allo-Thr-OH
CAS:Building block for the SPPS of kahalalide F. The hydroxyl group of D-aThr is involved in the ester bond of this cyclic depsipeptide.Formula:C19H19NO5Purity:99.7%Color and Shape:White PowderMolecular weight:341.36Fmoc-D-Allo-Thr-OH
CAS:(2R,3R)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-hydroxybutanoic acidFormula:C19H19NO5Purity:95%Molecular weight:341.36
