- Cbz-L-Lys(Cbz)-OH
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2026-06-05
- CAS:405-39-0
- Min. Order: 1kg
- Purity: 98%
- Supply Ability: 1T+
- Z-Lys(Z)-OH
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2022-02-22
- CAS:405-39-0
- Min. Order: 1KG
- Purity: 97.1%
- Supply Ability: 100 tons
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| | Z-Lys(Z)-OH Basic information |
| | Z-Lys(Z)-OH Chemical Properties |
| Melting point | 76-78°C | | Boiling point | 659.0±55.0 °C(Predicted) | | density | 1.238±0.06 g/cm3(Predicted) | | storage temp. | Sealed in dry,Room Temperature | | solubility | DMSO (Slightly), Methanol (Slightly) | | form | Solid | | pka | 3.97±0.21(Predicted) | | color | White to Off-White | | BRN | 1897206 | | Major Application | peptide synthesis | | InChIKey | BLZXFNUZFTZCFD-IBGZPJMESA-N | | SMILES | C(O)(=O)[C@H](CCCCNC(OCC1=CC=CC=C1)=O)NC(OCC1=CC=CC=C1)=O | | CAS DataBase Reference | 405-39-0(CAS DataBase Reference) |
| WGK Germany | 3 | | Storage Class | 11 - Combustible Solids |
| | Z-Lys(Z)-OH Usage And Synthesis |
| Chemical Properties | White Solid | | Uses | Protected L-lysine | | Definition | Z-Lys(Z)-OH is a lysine derivative.
| | reaction suitability | reaction type: solution phase peptide synthesis | | Synthesis | A 250 mL three-necked flask was loaded consecutively with water (20 mL), 1,4-dioxane (20 mL), and L-lysine (2.1 g, 14.4 mmol). The mixture was stirred until complete dissolution. The pH was adjusted to about 10.5 by the addition of 30% NaOH. Benzyl chloroformate (5.2 g, 30.6 mmol) was added while maintaining the pH at about 1011 by adding at the same time 30% NaOH. At the end of the addition, the reaction was stirred at 20° C. for about 1 hour. The pH was adjusted to 5 with 37% HCl. Ethyl acetate (30 mL) was added and the pH was adjusted to 1 with 37% HCl. The mixture was stirred at room temperature for about 30 minutes, the organic layer was separated and the aqueous layer was extracted with ethyl acetate (20 mL). The combined organic layer was washed with brine (30 mL) and dried over Na2SO4. Then, the solvent was evaporated to yield Z-Lys(Z)-OH as a yellowish oil (6.0 g, 99%). | | References | [1] Patent: US2006/94673, 2006, A1. Location in patent: Page/Page column 4
[2] Patent: CN106565771, 2017, A. Location in patent: Paragraph 0037; 0038; 0039
[3] Patent: CN106565772, 2017, A. Location in patent: Paragraph 0038
[4] Helvetica Chimica Acta, 1958, vol. 41, p. 1867,1876
[5] Journal of Biological Chemistry, 1935, vol. 111, p. 245,251 |
| | Z-Lys(Z)-OH Preparation Products And Raw materials |
| Raw materials | N6-Cbz-L-Lysine-->Thiosulfuric acid,anhydride with phenylmethyl carbonothioate, sodium salt (1:1)-->L-Lysine, N6-[(phenylmethoxy)carbonyl]-, methyl ester-->L-Lysine, N2,N6-bis[(phenylmethoxy)carbonyl]-, 1,1-dimethylethyl ester-->Carbonic acid, phenylmethyl 8-quinolinyl ester-->L-Lysine, N2,N6-bis[(phenylmethoxy)carbonyl]-, methyl ester-->4-HYDROXYPHENYLDIMETHYLSULFONIUM METHYL SULFATE-->CHLOROMETHYL BENZOATE-->L-Lysine-->Benzyl chloroformate | | Preparation Products | Z-LYS(Z)-ONP-->H-LYS-TYR-OH |
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