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Chemical Structure| 53363-89-6 Chemical Structure| 53363-89-6
Chemical Structure| 53363-89-6

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Boc-N-Me-Leu-OH is a protected N-methylleucine derivative with the amino group protected by tert-butoxycarbonyl (Boc), suitable for peptide synthesis.

4.5 *For Research Use Only !

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Product Details of Boc-N-Me-Leu-OH

CAS No. :53363-89-6
Formula : C12H23NO4
M.W : 245.32
SMILES Code : CC(C)C[C@H](N(C(OC(C)(C)C)=O)C)C(O)=O
MDL No. :MFCD00038522
InChI Key :YXJFAOXATCRIKU-VIFPVBQESA-N
Pubchem ID :7010555

Safety of Boc-N-Me-Leu-OH

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H335
Precautionary Statements:P261-P305+P351+P338

Application In Synthesis of Boc-N-Me-Leu-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 [ 53363-89-6 ]

[ 53363-89-6 ] Synthesis Path-Downstream   1~3

  • 1
  • [ 53363-89-6 ]
  • [ 17664-93-6 ]
  • C25H40N2O5 [ No CAS ]
  • 2
  • [ 16937-99-8 ]
  • [ 16948-16-6 ]
  • [ 53363-89-6 ]
  • C12H21NO4 [ No CAS ]
  • C12H21NO4 [ No CAS ]
  • C24H40NO4PolSi [ No CAS ]
  • [ 13734-31-1 ]
  • C53H88N7O7PolSi [ No CAS ]
  • 3
  • [ 53363-89-6 ]
  • [ 66866-69-1 ]
YieldReaction ConditionsOperation in experiment
62.1 g With hydrogenchloride; In dichloromethane; at 15℃; (3) Put 880mL of dichloromethane and 88.3g of N-methyl-Boc-L-leucine into a 2L reaction flask equipped with a thermometer at 15C, stir to dissolve and clear,Pass in hydrogen chloride gas very slowly. As the reaction progresses, the system slowly becomes turbid.A white solid precipitates out. After the raw material has reacted completely, filter it.Obtain 62.1g of N-methyl-L-leucine hydrochloride;
 

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