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Z-NVA-OH

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Z-NVA-OH Basic information

Product Name:
Z-NVA-OH
Synonyms:
  • BENZYLOXYCARBONYL-L-NORVALINE
  • Norvaline reference substance
  • CBZ-L-NORVALINE
  • Z-APE(2)-OH
  • Z-L-ALPHA-AMINOVALERIC ACID
  • Z-L-2-AMINOVALERIC ACID
  • Z-NVA-OH
  • Z-NORVALINE
CAS:
21691-44-1
MF:
C13H17NO4
MW:
251.28
EINECS:
1533716-785-6
Product Categories:
  • Peptide
Mol File:
21691-44-1.mol
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Z-NVA-OH Chemical Properties

Boiling point:
439.4±38.0 °C(Predicted)
Density 
1.184±0.06 g/cm3(Predicted)
storage temp. 
Sealed in dry,2-8°C
solubility 
Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
form 
Powder
pka
4.00±0.20(Predicted)
CAS DataBase Reference
21691-44-1(CAS DataBase Reference)
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Safety Information

HS Code 
2922498590
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Z-NVA-OH Usage And Synthesis

Uses

Z-NVA-OH is also known as Cbz-L-norvaline. It could be used to synthesise Z-Nva-Ser(Bu’)-Gly-OPh. In specific steps, as follows: the protected dipeptide(53.1 g. 124mM) and Tos.OH.H2O (33.6g. 124mM) were dissolved in DMF (200) and hydrogenolysed overnight in the presence of 10% Pd/C (6g), then filtered and concentrated to 100ml. Z-Nva-OH (37.4g. 149mM) was dissolved in CH2Cl2 (170ml) and NMM (16.4ml. 149mM) added. After cooling to -20℃, pivaloyl chloride (17.8ml. 145 mM) was added, and the solution was stirred for 20 minutes before the precooled DMF solution from above was added. Following the addition of NMM (13.6 ml, 124 mM), the reaction was stirred at - 20℃ for 3 hr, then maintained at room temperature overnight. The solution was evaporated, and the product dissolved in EtOAc. Washing with acid and base in the usual way, followed by crystallisation from EtOAc/petroleum ether yielded Z-Nva-Ser(Bu’)-Gly-OPh[1].

References

[1] I.J. Galpin. “Peptides—XXXXII.” Tetrahedron 37 17 (1981): Pages 3017-3023.

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