- Boc-D-Glu(Obzl)-OH
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- $0.00/ kg
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2026-03-31
- CAS:35793-73-8
- Min. Order: 1kg
- Purity: 98%
- Supply Ability: 1T+
- Boc-D-Glu(Obzl)-Obzl
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- $1.00 / 1g
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2020-01-06
- CAS:35793-73-8
- Min. Order: 1g
- Purity: 98%
- Supply Ability: 100KG
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| | Boc-D-Glutamic acid 5-benzyl ester Basic information |
| Product Name: | Boc-D-Glutamic acid 5-benzyl ester | | Synonyms: | BOC-GLUTAMIC ACID(OBZL)-OH;BOC-GLU(OBZL)-OH;BOC-L-GLUTAMIC ACID G-BENZYL ESTER;BOC-L-GLUTAMIC ACID (OBZL);BOC-L-GLUTAMIC ACID GAMMA-BENZYL ESTER;BOC-L-GLU(BZL)-OH;BOC-L-GLU(OBZL)-OH;T-BUTYLOXYCARBONYL-L-GLUTAMIC ACID GAMMA-BENZYL ESTER | | CAS: | 35793-73-8 | | MF: | C17H23NO6 | | MW: | 337.37 | | EINECS: | 237-007-5 | | Product Categories: | Amino Acid Derivatives | | Mol File: | 35793-73-8.mol |  |
| | Boc-D-Glutamic acid 5-benzyl ester Chemical Properties |
| Melting point | 69-71 °C | | alpha | 5.5 º (c=1% in acetic acid) | | Boiling point | 522.6±50.0 °C(Predicted) | | density | 1+-.0.06 g/cm3(Predicted) | | storage temp. | Sealed in dry,2-8°C | | pka | 3.81±0.10(Predicted) | | form | solid | | color | White | | Major Application | peptide synthesis | | InChI | 1S/C17H23NO6/c1-17(2,3)24-16(22)18-13(15(20)21)9-10-14(19)23-11-12-7-5-4-6-8-12/h4-8,13H,9-11H2,1-3H3,(H,18,22)(H,20,21)/t13-/m1/s1 | | InChIKey | AJDUMMXHVCMISJ-CYBMUJFWSA-N | | SMILES | N([C@H](CCC(=O)OCc1ccccc1)C(=O)O)C(=O)OC(C)(C)C | | CAS DataBase Reference | 35793-73-8(CAS DataBase Reference) |
| Safety Statements | 22-24/25 | | WGK Germany | 3 | | HS Code | 2922500090 | | Storage Class | 11 - Combustible Solids |
| | Boc-D-Glutamic acid 5-benzyl ester Usage And Synthesis |
| Uses | Boc-Glu(OBzl)-OH, is an amino acid building block used in peptide synthesis. With a growing peptide drug market the fast, reliable synthesis of peptides is of great importance. | | reaction suitability | reaction type: Boc solid-phase peptide synthesis | | Synthesis | (R)-2-Amino-5-(benzyloxy)-5-oxovaleric acid (6.0 g, 25.3 mmol) was used as a starting material, which was dissolved in a mixed solvent of dioxane and water (1:1, 40 mL). To this solution was added di-tert-butyl dicarbonate (Boc2O, 6.62 g, 30.36 mmol) at 0 °C. The reaction mixture was stirred at room temperature for 16 hours. After completion of the reaction, the solvent was removed by distillation under reduced pressure. The residue was diluted with 30 mL of water and alkalized with sodium carbonate (Na2CO3). Subsequently, the aqueous layer was washed with ethyl acetate (EtOAc, 3 x 100 mL). The aqueous layer was adjusted to pH 2-3 with 5 M HCl aqueous solution and then extracted with ethyl acetate (EtOAc, 4 × 100 mL). The organic extracts were combined, washed with brine and dried with anhydrous sodium sulfate (Na2SO4). Finally, the solvent was removed by distillation under reduced pressure to afford the target product (R)-5-(benzyloxy)-2-((tert-butoxycarbonyl)amino)-5-oxopentanoic acid [Compound 3j, 8.19 g, 96% yield] as a viscous, colorless oil. The product was structurally confirmed by nuclear magnetic resonance hydrogen spectroscopy (1H NMR, CDCl3) and electrospray mass spectrometry (ESI MS). | | References | [1] Patent: WO2017/98529, 2017, A1. Location in patent: Page/Page column 18; 32
[2] Patent: EP2612857, 2017, B1. Location in patent: Paragraph 0123-0124
[3] Organic and Biomolecular Chemistry, 2007, vol. 5, # 12, p. 1915 - 1923
[4] Chinese Chemical Letters, 2011, vol. 22, # 12, p. 1443 - 1446 |
| | Boc-D-Glutamic acid 5-benzyl ester Preparation Products And Raw materials |
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