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Chemical Structure| 17791-52-5 Chemical Structure| 17791-52-5
Chemical Structure| 17791-52-5

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Boc-His-OH is a histidine derivative, commonly used in biochemical research and drug synthesis.

Synonyms: N-tert-Butyloxycarbonyl-L-histidine

4.5 *For Research Use Only !

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Product Details of Boc-His-OH

CAS No. :17791-52-5
Formula : C11H17N3O4
M.W : 255.27
SMILES Code : CC(C)(C)OC(=O)N[C@@H](CC1=CN=CN1)C(O)=O
Synonyms :
N-tert-Butyloxycarbonyl-L-histidine
MDL No. :MFCD00065576
InChI Key :AYMLQYFMYHISQO-QMMMGPOBSA-N
Pubchem ID :87308

Safety of Boc-His-OH

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

Application In Synthesis of Boc-His-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 [ 17791-52-5 ]

[ 17791-52-5 ] Synthesis Path-Downstream   1~7

  • 2
  • [ 19887-32-2 ]
  • [ 104882-10-2 ]
  • [ 17791-52-5 ]
  • {(S)-1-[(S)-1-((1S,2R,3S)-1-Cyclohexylmethyl-2,3-dihydroxy-5-methyl-hexylcarbamoyl)-2-(1H-imidazol-4-yl)-ethylcarbamoyl]-2-phenyl-ethyl}-carbamic acid ethyl ester [ No CAS ]
  • 3
  • [ 19887-32-2 ]
  • [ 117248-32-5 ]
  • [ 17791-52-5 ]
  • {(S)-1-[(S)-1-((1S,2R,3S)-1-Cyclohexylmethyl-2,3-dihydroxy-pentylcarbamoyl)-2-(1H-imidazol-4-yl)-ethylcarbamoyl]-2-phenyl-ethyl}-carbamic acid ethyl ester [ No CAS ]
  • 5
  • [ 13139-16-7 ]
  • [ 7536-55-2 ]
  • [ 2488-17-7 ]
  • [ 13726-85-7 ]
  • [ 13734-34-4 ]
  • [ 13836-37-8 ]
  • [ 54613-99-9 ]
  • [ 13139-14-5 ]
  • [ 17791-52-5 ]
  • HFRWRQIKIWFQNRRM[O]KWKK-NH2 [ No CAS ]
YieldReaction ConditionsOperation in experiment
General procedure: All protected amino acids were coupled in CH2Cl2 (5 ml) using DCC (2.5 equiv.) and HOBt (2.5 equiv.) until completion (3 h) judged by Kaiser [15] ninhydrin test. After coupling of the appropriate amino acid, Boc deprotection was effected by use of TFA/CH2Cl2 (1:1, 5 ml)) for 5 min first then repeated for 25 min. Following neutralization with 10% TEA/CH2Cl2 three times (5-5 ml of each), the synthetic cycle was repeated to assemble the resin-bond protected peptide. The peptides were cleaved from the resin with simultaneous side chain deprotection by acidolysis with anhydrous hydrogen fluoride (5 ml) containing 2% anisole, 8% dimethyl sulfide and indole at 5 C for 45 min. The crude peptides were dissolved in aqueous acetic acid and lyophilized.
  • 6
  • [ 17791-52-5 ]
  • [ 22888-59-1 ]
  • [ 1184963-21-0 ]
  • 7
  • [ 17791-52-5 ]
  • [ 22888-59-1 ]
  • [ 1185192-61-3 ]
 

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