Basic information Safety Supplier Related

BOC-LEU-GLY-OH

Basic information Safety Supplier Related

BOC-LEU-GLY-OH Basic information

Product Name:
BOC-LEU-GLY-OH
Synonyms:
  • BOC-LEU-GLY-OH
  • N-[(1,1-Dimethylethoxy)carbonyl]-L-leucylglycine
  • Boc-L-Leu-Gly-OH
  • N-(tert-Butoxycarbonyl)-L-leucylglycine
  • (S)-2-(2-((tert-Butoxycarbonyl)aMino)-4-MethylpentanaMido)acetic acid
  • tert-(Butyloxycarbonyl)leucylglycine
  • Boc-Leu-Gly-OH≥ 99% (TLC)
  • (Tert-Butoxy)Carbonyl Leu-Gly-OH
CAS:
32991-17-6
MF:
C13H24N2O5
MW:
288.34
Mol File:
32991-17-6.mol
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BOC-LEU-GLY-OH Chemical Properties

Boiling point:
499.6±30.0 °C(Predicted)
Density 
1.122±0.06 g/cm3(Predicted)
storage temp. 
Sealed in dry,2-8°C
form 
Solid
pka
3.42±0.10(Predicted)
color 
White to off-white
optical activity
Consistent with structure
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Safety Information

HazardClass 
IRRITANT
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BOC-LEU-GLY-OH Usage And Synthesis

Chemical Properties

White powder

Uses

N-[N-[(1,1-Dimethylethoxy)carbonyl]-L-leucyl]-glycine is used to prepare aziridinedicarboxylic acid peptides as cysteine protease inhibitors. It is also used to prepare dipeptide monoester prodrugs of floxuridine with enhanced cancer cell growth inhibition.

Synthesis

27610-07-7

32991-17-6

General procedure for the synthesis of (S)-2-(2-((tert-butoxycarbonyl)amino)-4-methylpentanamido)acetic acid from (tert-butoxycarbonyl)-L-leucylglycine methyl ester: Compound 9a (2.6 g, 10 mmol) was dissolved in 50 mL of methanol, 1 M NaOH solution (30 mL) was added, and the reaction was stirred for 3 h at room temperature. Upon completion of the reaction, the solvent was removed by vacuum concentration and the pH of the residue was adjusted to 2-3 with 1 M HCl. Subsequently, the mixture was extracted three times with ethyl acetate (EtOAc). The organic phases were combined and dried over anhydrous sodium sulfate (Na2SO4). After filtration, ethyl acetate was evaporated under reduced pressure to give compound 10a as a white solid in 92.4% yield.

References

[1] Bioorganic and Medicinal Chemistry, 2014, vol. 22, # 11, p. 3055 - 3064
[2] Zeitschrift fur Naturforschung - Section B Journal of Chemical Sciences, 2009, vol. 64, # 2, p. 237 - 244
[3] Bioorganic and Medicinal Chemistry, 2010, vol. 18, # 2, p. 887 - 895

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