BOC-VAL-GLY-OH
BOC-VAL-GLY-OH Basic information
- Product Name:
- BOC-VAL-GLY-OH
- Synonyms:
-
- BOC-VAL-GLY-OH
- Butoxycarbonyl L-valinyl-glycine
- Boc-L-Val-Gly-OH
- Boc-Val-Gly-OH≥ 95% (HPLC)
- (Tert-Butoxy)Carbonyl Val-Gly-OH
- 2-[(2S)-2-{[(tert-butoxy)carbonyl]amino}-3-methylbutanamido]acetic acid
- Boc-Val-Gly
- (tert-Butoxycarbonyl)-L-valylglycine
- CAS:
- 45233-75-8
- MF:
- C12H22N2O5
- MW:
- 274.31
- Mol File:
- 45233-75-8.mol
BOC-VAL-GLY-OH Chemical Properties
- Melting point:
- 100-110°C
- Boiling point:
- 491.2±30.0 °C(Predicted)
- Density
- 1.141±0.06 g/cm3(Predicted)
- storage temp.
- 2-8°C
- form
- Solid
- pka
- 3.40±0.10(Predicted)
- color
- White to off-white
BOC-VAL-GLY-OH Usage And Synthesis
Chemical Properties
White powder
Uses
peptide synthesis
reaction suitability
reaction type: Boc solid-phase peptide synthesis
Synthesis
51803-69-1
45233-75-8
GENERAL METHOD: Methyl tert-butoxycarbonyl-L-valylaminoacetate (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 evaporation and the residue was adjusted to pH 2-3 with 1 M HCl. Subsequently, the mixture was extracted three times with EtOAc, the organic phases were combined and dried with anhydrous Na2SO4. Finally, the EtOAc was evaporated to afford the target compound 10a as a white solid in 92.4% yield.
References
[1] Journal of the American Chemical Society, 2010, vol. 132, # 13, p. 4577 - 4579
[2] Bioorganic and Medicinal Chemistry, 2014, vol. 22, # 11, p. 3055 - 3064
[3] Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999), 1992, # 7, p. 1187 - 1193
[4] Journal of Medicinal Chemistry, 1995, vol. 38, # 20, p. 4014 - 4018
BOC-VAL-GLY-OHSupplier
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