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Chemical Structure| 13726-67-5 Chemical Structure| 13726-67-5
Chemical Structure| 13726-67-5

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Boc-Asp-OH is a protected L-aspartic acid derivative with the amino group protected by tert-butoxycarbonyl (Boc), commonly used in peptide synthesis and biochemical research.

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Product Details of Boc-Asp-OH

CAS No. :13726-67-5
Formula : C9H15NO6
M.W : 233.22
SMILES Code : O=C(O)[C@@H](NC(OC(C)(C)C)=O)CC(O)=O
MDL No. :MFCD00037279
InChI Key :KAJBMCZQVSQJDE-YFKPBYRVSA-N
Pubchem ID :99718

Safety of Boc-Asp-OH

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

Application In Synthesis of Boc-Asp-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 [ 13726-67-5 ]

[ 13726-67-5 ] Synthesis Path-Downstream   1~7

  • 1
  • [ 67-56-1 ]
  • [ 13726-67-5 ]
  • [ 98045-03-5 ]
  • 2
  • [ 13726-67-5 ]
  • [ 29390-67-8 ]
  • C93H153N3O72 [ No CAS ]
  • 3
  • [ 186581-53-3 ]
  • [ 13726-67-5 ]
  • [ 130622-08-1 ]
  • 4
  • [ 67-56-1 ]
  • [ 13726-67-5 ]
  • [ 130622-08-1 ]
  • 5
  • [ 13726-67-5 ]
  • [ 128427-10-1 ]
  • 6
  • [ 13726-67-5 ]
  • [ 74-88-4 ]
  • [ 130622-08-1 ]
YieldReaction ConditionsOperation in experiment
99% With sodium chloride; potassium carbonate; In water; Reference Example 2-23 Synthesis of (2S)-2-amino-4-[(4-chlorobenzyl)thio]butanol (Reference Compound No. 2-23): 40.1 g (0.4 mol) of potassium carbonate was added to an anhydrous dimethylformamide solution containing 23.4 g (0.1 mol) of t-butoxycarbonyl-L-aspartic acid. The above prepared mixture was stirred at room temperature for 2 hours, and then 31.1 ml (0.5 mol) of methyl iodide was added dropwise thereto. The reaction mixture was further stirred overnight and water was then added thereto, followed by the extraction with ethyl acetate. The resultant organic extract layer was washed with 1 N hydrochloric acid, a saturated aqueous solution of sodium chloride, and dried over anhydrous sodium sulfate. The solvent was concentrated under reduced pressure, whereby 25.8 g of L-t-butoxycarbonylaspartic acid dimethyl ester was obtained in a yield of 99%.
  • 7
  • [ 13726-67-5 ]
  • [ 2886-33-1 ]
  • [ 1186099-20-6 ]
 

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