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Chemical Structure| 957780-56-2 Chemical Structure| 957780-56-2
Chemical Structure| 957780-56-2

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Synonyms: Fmoc-Glu(OtBu)-Thr(psi(Me,Me)pro)-OH

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Product Details of Fmoc-Glu(OtBu)-Thr(psi(Me,Me)pro)-OH

CAS No. :957780-56-2
Formula : C31H38N2O8
M.W : 566.64
SMILES Code : C[C@H]1OC(C)(N(C([C@@H](NC(OCC2C3=C(C4=C2C=CC=C4)C=CC=C3)=O)CCC(OC(C)(C)C)=O)=O)[C@@H]1C(O)=O)C
Synonyms :
Fmoc-Glu(OtBu)-Thr(psi(Me,Me)pro)-OH
MDL No. :MFCD18427360
InChI Key :SIDKUUFAHNZJLW-VAQLEPBLSA-N
Pubchem ID :75534989

Safety of Fmoc-Glu(OtBu)-Thr(psi(Me,Me)pro)-OH

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H335
Precautionary Statements:P261-P280-P301+P312-P302+P352-P305+P351+P338

Application In Synthesis of Fmoc-Glu(OtBu)-Thr(psi(Me,Me)pro)-OH

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Downstream synthetic route of [ 957780-56-2 ]

[ 957780-56-2 ] Synthesis Path-Downstream   1~1

  • 1
  • N-alpha-Fmoc-N-beta-O-t-butyl-L-aspartyl-N-α-(2,4-dimethoxybenzyl)glycine [ No CAS ]
  • [ 29022-11-5 ]
  • [ 68858-20-8 ]
  • [ 35661-60-0 ]
  • [ 13734-34-4 ]
  • [ 957780-56-2 ]
  • [ 35661-39-3 ]
  • [ 920519-33-1 ]
  • (2S)-N-((9H-fluoren-9-ylmethyloxy)carbonyl)aspartic acid-4-((3-ethyl)pent-3-yl) ester [ No CAS ]
  • Fmoc-Gly-Ser(ψMe,MePro)-OH [ No CAS ]
  • Fmoc-Gln(Trt)-Thr(ψMe,MePro)-OH [ No CAS ]
  • [ 71989-31-6 ]
  • [ 35661-40-6 ]
  • [ 71989-33-8 ]
  • [ 71989-14-5 ]
  • [ 71989-18-9 ]
  • [ 71989-23-6 ]
  • [ 71989-38-3 ]
  • [ 71989-26-9 ]
  • [ 103213-32-7 ]
  • [ 71989-35-0 ]
  • [ 132388-59-1 ]
  • [ 132327-80-1 ]
  • [ 86060-81-3 ]
  • [ 109425-51-6 ]
  • [ 77284-32-3 ]
  • Nα-(9-fluorenylmethyloxycarbonyl)-Nγ-2,2,4,6,7-pentamethyldihydrobenzofuran-5-sulfonyl-L-arginine [ No CAS ]
  • [Cys105,Nle125,170,Cys(Acm)165,182,189,Asn107,Asp109](105-191)hGH-NH2 [ No CAS ]
YieldReaction ConditionsOperation in experiment
101.1 mg General procedure: The syntheses of the fragments were performed on an automatic peptide synthesizer under microwave conditions using an 8-fold excess of 0.5 M amino acids, 0.5 M HATU/NMP, 2 M DIEA /NMP or 1.0 M DIC/NMP and 0.5 M Oxyma /NMP. The final concentration of Fmoc-amino acids was 0.2 M. The coupling cycles were conducted according to Table 1. Fmoc deprotection was carried out using 35% piperidine/NMP containing 0.1 M HOBt at room temperature for 2 and 6 min, followed by 4 min at 48 C.
 

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