| Identification | Back Directory | [Name]
Z-PHE-ALA-OH | [CAS]
21881-18-5 | [Synonyms]
Z-PHE-ALA
Z-PHE-ALA-OH
CBZ-L-PHE-ALA
N-CBZ-PHE-ALA
Cbz-Phe-Ala-OH
CBZ-L-PHE-L-ALA
Cbz-L-Phe-L-Ala-OH
Z-PHE-ALA-OH USP/EP/BP
Z-Phe-Ala-OH≥ 99% (HPLC)
N-carbobenzyloxy-Phe-Ala
Z-L-PHENYLALANYL-L-ALANINE
N-CARBOBENZOXY-L-PHENYLALANYL-L-ALANINE
N-Cbz-Phe-Ala, Z-L-phenylalanyl-L-alanine
N-BENZYLOXYCARBONYL-L-PHENYLALANYL-L-ALANINE
L-Alanine, N-[(phenylmethoxy)carbonyl]-L-phenylalanyl-
(S)-2-((S)-2-(((Benzyloxy)carbonyl)aMino)-3-phenylpropanaMido)propanoic acid | [Molecular Formula]
C20H22N2O5 | [MDL Number]
MFCD00037237 | [MOL File]
21881-18-5.mol | [Molecular Weight]
370.4 |
| Chemical Properties | Back Directory | [Melting point ]
151-154 °C | [storage temp. ]
Sealed in dry,2-8°C | [solubility ]
methanol: ~50mg/mL, almost clear, almost colorless | [Boiling point ]
666.1±55.0 °C(Predicted) | [density ]
1.253±0.06 g/cm3(Predicted) | [form ]
powder | [pka]
3.50±0.10(Predicted) | [InChI]
1S/C20H22N2O5/c1-14(19(24)25)21-18(23)17(12-15-8-4-2-5-9-15)22-20(26)27-13-16-10-6-3-7-11-16/h2-11,14,17H,12-13H2,1H3,(H,21,23)(H,22,26)(H,24,25)/t14-,17-/m0/s1 | [InChIKey]
LEJTXQOVOPDGHS-YOEHRIQHSA-N | [SMILES]
C[C@H](NC(=O)[C@H](Cc1ccccc1)NC(=O)OCc2ccccc2)C(O)=O |
| Hazard Information | Back Directory | [Chemical Properties]
White to off-white powder | [Uses]
Sensitive substrate for cathepsin A. | [Synthesis]
The general procedure for the synthesis of the compound (CAS:3338-39-4) from (S)-2,5-dioxopyrrolidin-1-yl 2-(((benzyloxy)carbonyl)amino)-3-phenylpropanoate and L-alanine was as follows: with reference to the method of Itoh [M. Itoh, Chem. Pharm. Bull., 20, 664 (1972)], to L- alanine (18 mmol, 1.60 g) dissolved in 200 mL of a 1:1 dioxane-water mixture to triethylamine (36 mmol, 5.0 mL). Solid carbon dioxide tablets were added under stirring conditions until the solution pH reached 8. Subsequently, N-Benzyloxycarbonyl-L-phenylalanine N-hydroxysuccinimide ester (18 mmol, 7.13 g) was added under stirring at room temperature. After 16-20 hours of reaction, the reaction mixture was acidified by slow addition of 1N HCl followed by extraction with ethyl acetate. The organic phase was separated, washed sequentially with water (twice) and brine, dried over MgSO4, concentrated by rotary evaporation and dried under high vacuum to give 6.19 g (93% yield) of N-Benzyloxycarbonyl-L-phenylalanyl-L-alanine as a white solid with a melting point of 160-164 °C (literature value: 165 °C; G.R. Pettit, 'Synthetic Peptides', Vol. 1, p. 141 (1970)). Using similar methods, the following compounds of formula (2) can be prepared according to the procedure described in Preparation 1. | [References]
[1] Bioorganic and Medicinal Chemistry, 2010, vol. 18, # 17, p. 6230 - 6237
[2] Patent: US5055451, 1991, A
[3] Bioorganic and Medicinal Chemistry, 2009, vol. 17, # 3, p. 1071 - 1078 |
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Spectrum Chemical Manufacturing Corp.
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021-021-021-67601398-809-809-809 15221380277 |
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www.spectrumchemical.com/oa_html/index.jsp?minisite=10020&respid=22372&language=us |
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