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Fmoc-Ser(tBu)-Gly-OH

Fmoc-Ser(tBu)-Gly-OH ??? ???
?? ??:
81672-17-5
???:
Fmoc-Ser(tBu)-Gly-OH
???(??):
Fmoc-ser(tbu)-Gly;Fmoc-Ser(tBu)-Gly-OH;(N-Fmoc-O-tert-butyl-L-seryl)-glycine;(9H-Fluoren-9-yl)MethOxy]Carbonyl Ser(tBu)-Gly-OH;N-(((9H-fluoren-9-yl)methoxy)carbonyl)-O-(tert-butyl)-L-serylglycine;Glycine, O-(1,1-dimethylethyl)-N-[(9H-fluoren-9-ylmethoxy)carbonyl]-L-seryl-;2-[(2S)-3-(tert-butoxy)-2-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)propanamido]acetic acid
CBNumber:
CB53369149
???:
C24H28N2O6
??? ??:
440.49
MOL ??:
81672-17-5.mol

Fmoc-Ser(tBu)-Gly-OH ??

?? ?
703.1±60.0 °C(Predicted)
??
1.243±0.06 g/cm3(Predicted)
?? ?? (pKa)
3.29±0.10(Predicted)
InChIKey
KXWFIADQSGXDHH-FQEVSTJZSA-N
SMILES
C(O)(=O)CNC(=O)[C@H](COC(C)(C)C)NC(OCC1C2=C(C=CC=C2)C2=C1C=CC=C2)=O

??

HS ?? 2924297099

Fmoc-Ser(tBu)-Gly-OH C??? ??, ??, ??

??

Fmoc-Ser(tBu)-Gly-OH serves as a building block in the synthesis of peptides. The Fmoc group acts as a protective group, allowing for selective deprotection and subsequent coupling reactions during solid-phase peptide synthesis. Fmoc is often preferred over Boc because of its ease of cleavage.

Fmoc-Ser(tBu)-Gly-OH ?? ?? ? ???

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Fmoc-Ser(tBu)-Gly-OH ?? ??

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