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Chemical Structure| 90600-20-7 Chemical Structure| 90600-20-7
Chemical Structure| 90600-20-7

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Synonyms: (S)-2-((tert-Butoxycarbonyl)amino)pent-4-enoic acid

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Product Details of Boc-Allyl-Gly-OH

CAS No. :90600-20-7
Formula : C10H17NO4
M.W : 215.25
SMILES Code : C=CC[C@H](NC(OC(C)(C)C)=O)C(O)=O
Synonyms :
(S)-2-((tert-Butoxycarbonyl)amino)pent-4-enoic acid
MDL No. :MFCD01320851
InChI Key :BUPDPLXLAKNJMI-ZETCQYMHSA-N
Pubchem ID :2734487

Safety of Boc-Allyl-Gly-OH

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

Application In Synthesis of Boc-Allyl-Gly-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 [ 90600-20-7 ]

[ 90600-20-7 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 90600-20-7 ]
  • [ 2133-34-8 ]
  • [ 90599-96-5 ]
YieldReaction ConditionsOperation in experiment
93% 1.6g (7.4 mmol) of Boc-L-allylglycine was dissolved in methanol (25 ml), followed by bubbling with ozone gas at -78 C. After bubbling until color of the solution turned blue, oxygen was bubbled until the blue color disappeared. After returning to room temperature, 752 mg (7.4 mmol) of <strong>[2133-34-8]L-azetidine-2-carboxylic acid</strong> and 470 mg (7.4 mmol) of sodium cyanoborohydride were added, followed by stirring for one hour. After vacuum concentration of the reaction mixture, 2.1 g of compound (3-3) (yield 93%) was obtained by short-pass silica gel chromatography with silica gel (after removing the residue of sodium cyanoborohydride and a small amount of byproduct derived from L-allylglycine with a mobile phase: a mixture solution of ethyl acetate: methanol = 5:1 (v/v), methanol solution was passed through).
 

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