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Chemical Structure| 33305-77-0 Chemical Structure| 33305-77-0
Chemical Structure| 33305-77-0

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Boc-Glu(OBzl)-OH is a glutamic acid derivative, used for peptide synthesis, increasing the hydrophilicity of peptides and playing an important role in structure and receptor binding.

Synonyms: (S)-2-((tert-Butoxycarbonyl)amino)-3-(4-nitrophenyl)propanoic acid

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Product Details of Boc-Phe(4-NO2)-OH

CAS No. :33305-77-0
Formula : C14H18N2O6
M.W : 310.30
SMILES Code : O=C(O)[C@@H](NC(OC(C)(C)C)=O)CC1=CC=C([N+]([O-])=O)C=C1
Synonyms :
(S)-2-((tert-Butoxycarbonyl)amino)-3-(4-nitrophenyl)propanoic acid
MDL No. :MFCD00038128

Safety of Boc-Phe(4-NO2)-OH

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

Application In Synthesis of Boc-Phe(4-NO2)-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 [ 33305-77-0 ]

[ 33305-77-0 ] Synthesis Path-Downstream   1~3

  • 1
  • [ 33305-77-0 ]
  • [ 180683-64-1 ]
  • [ 199336-09-9 ]
  • 3
  • [ 33305-77-0 ]
  • [ 23357-46-2 ]
  • tert-butyl((S)-3-(4-nitrophenyl)-1-oxo-1-(((R)1,2,3,4-tetrahydronaphthalen-1-yl)amino)propan-2-yl)carbamate [ No CAS ]
YieldReaction ConditionsOperation in experiment
70% To a solution of (S)-2-((tert-butoxycarbonyl) amino)-3-(4-nitrophenyl)propanoic acid (1.15 g, 3.71 mmol) in DMF (6 mE) were added EDC (1.0 g, 5.19 mmol) and 3H-[ 1 ,2,3]triazolo[4,5-b]pyridin-3-ol (0.50 g, 3.71 mmol). The reaction mixture was stirred at it for 5 mm, and treated with a solution of (R)-1,2,3,4-tetrahydronaphthalen- 1-amine (0.60 g, 4.08 mmol) in DMF (3 mE) and DIEA (1.30 mE, 7.41 mmol). The resulting mixture was stirred at it for 1 h. The reaction mixture was diluted with ethyl acetate and brine. The organic layer was separated and washed with saturated aq. NaHCO3 solution and brine successively. The organic layer was separated and dried over MgSO4. The filtrate was concentrated in vacuo and the residue was residue was purified by flash column chromatography (gradient elution from 0 to 20% of ethyl acetate/DCM) to afford the title compound (1.13 g, 70%) as a white solid. MS(ESI) mlz 440.3 (M+H).
 

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