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Fmoc-(S)-Asu(OtBu)-OH

Fmoc-(S)-Asu(OtBu)-OH is a protected amino acid derivative used in solid-phase peptide synthesis. Its orthogonal protecting groups support selective deprotection strategies. Researchers utilize it to incorporate Asu residues into custom sequences. The molecule contributes to expanding synthetic peptide chemistry.

Designed for biological research and industrial applications, not intended for individual clinical or medical purposes.
Fmoc-(S)-Asu(OtBu)-OH(CAS 276869-41-1)

CAT No: Q-OS-0033

CAS No:276869-41-1

Synonyms/Alias:276869-41-1;Fmoc-Asu(OtBu)-OH;(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-8-(tert-butoxy)-8-oxooctanoic acid;(2S)-2-(9H-fluoren-9-ylmethoxycarbonylamino)-8-[(2-methylpropan-2-yl)oxy]-8-oxooctanoic acid;(S)-2-(((9H-fluoren-9-yl)methoxy)carbonylamino)-8-tert-butoxy-8-oxooctanoic acid;MFCD00080269;(2S)-8-(tert-butoxy)-2-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)-8-oxooctanoic acid;(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)-amino)-8-(tert-butoxy)-8-oxooctanoic acid;(S)-Fmoc-2-Aminooctanedioic acid 8-tert-butyl ester;(2S)-8-(TERT-BUTOXY)-2-{[(9H-FLUOREN-9-YLMETHOXY)CARBONYL]AMINO}-8-OXOOCTANOIC ACID;SCHEMBL16061105;C27H33NO6;DTXSID80678867;(S)-2-FMOC-AMINO-OCTANEDIOIC ACID 8-TERT-BUTYL ESTER;AKOS005063575;AKOS016004540;GS-5421;DB-001134;CS-0101064;F12310;(S)-2-Fmoc-amino-8-(tert-butoxy)-8-oxooctanoic acid;(2S)-8-tert-Butoxy-2-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)-8-oxooctanoic acid;(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-8-(tert-butoxy)-8-oxooctanoicacid;

Custom Peptide Synthesis
cGMP Peptide
  • Registration of APIs
  • CMC information required for an IND
  • IND and NDA support
  • Drug master files (DMF) filing
M.F/Formula
C27H33NO6
M.W/Mr.
467.6
Sequence
Three Letter Code:Fmoc-Asu(OtBu)(OtBu)-OH
Application
Peptide synthesis; Drug screening
Purity
97%min
InChI
InChI=1S/C27H33NO6/c1-27(2,3)34-24(29)16-6-4-5-15-23(25(30)31)28-26(32)33-17-22-20-13-9-7-11-18(20)19-12-8-10-14-21(19)22/h7-14,22-23H,4-6,15-17H2,1-3H3,(H,28,32)(H,30,31)/t23-/m0/s1
InChI Key
ULPCAXORIFXUMN-QHCPKHFHSA-N

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