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Chemical Structure| 5854-78-4 Chemical Structure| 5854-78-4
Chemical Structure| 5854-78-4

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H-Thr(tBu)-OtBu is a threonine derivative, commonly used in peptide synthesis and drug development.

Synonyms: O-tert-Butylthreoninetert-butyl ester

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Product Details of H-Thr(tBu)-OtBu

CAS No. :5854-78-4
Formula : C12H25NO3
M.W : 231.33
SMILES Code : C[C@@H](OC(C)(C)C)[C@H](N)C(OC(C)(C)C)=O
Synonyms :
O-tert-Butylthreoninetert-butyl ester
MDL No. :MFCD00077109
InChI Key :PPDIUNOGUIAFLV-BDAKNGLRSA-N
Pubchem ID :7018832

Safety of H-Thr(tBu)-OtBu

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H315-H319-H335
Precautionary Statements:P261-P305+P351+P338

Application In Synthesis of H-Thr(tBu)-OtBu

* 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 [ 5854-78-4 ]

[ 5854-78-4 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 2483-51-4 ]
  • [ 5854-78-4 ]
  • C26H41N3O7 [ No CAS ]
YieldReaction ConditionsOperation in experiment
84% With 2,2':6',2'':6'',2'''-quaterpyridine; pentamethoxy tantalum; at 70℃; for 48h; Amide compounds were produced by reacting an aminoester compound with an amino compound under the respective reaction conditions below in the presence of a Ta(OMe)5 catalyst and a ligand. The yield for each product is indicated below the formula. In the reaction formula below, L-ala represents an L-alanine residue, Val represents an L-valine residue, Leu represents an L-Leucine residue, ILe represents an L-isoleucine residue, Gly represents glycine residue, Phe represents an L-phenylalanine residue, and Thr(OtBu) represents O-(tert butyl) L-threonine residue.
 

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