N-ALPHA, N-DELTA-BIS(BENZYLOXYCARBONYL)-L-ORNITHINE
N'2,N'5-dibenzyloxycarbonyl-L-ornithine
CAS: 2274-58-0
Molecular Formula: C21H24N2O6
N-ALPHA, N-DELTA-BIS(BENZYLOXYCARBONYL)-L-ORNITHINE - Names and Identifiers
| Name | N'2,N'5-dibenzyloxycarbonyl-L-ornithine |
| Synonyms | Z-Orn(Z)-OH Z-L-ORN(Z)-OH Z-ORNITHINE(Z)-OH C21H24N2O6·C12H23N N-a-CBZ-(N-d-CBZ)-L-Orn N,N'-Bis-Cbz-L-ornithine N-α,N-δ-di-Z-L-ornithine N-ALPHA,DELTA-BIS-Z-L-ORNITHINE N-ALPHA,N-DELTA-DI-CBZ-L-ORNITHINE N'2,N'5-dibenzyloxycarbonyl-L-ornithine N-ALPHA,N-DELTA-DICARBOBENZOXY-L-ORNITHINE N~2~,N~5~-bis[(benzyloxy)carbonyl]ornithine N~2~,N~5~-bis[(benzyloxy)carbonyl]-L-ornithine N-ALPHA, N-DELTA-DIBENZYLOXYCARBONYL-L-ORNITHINE N-ALPHA, N-DELTA-BIS(BENZYLOXYCARBONYL)-L-ORNITHINE |
| CAS | 2274-58-0 |
| EINECS | 218-889-0 |
| InChI | InChI=1/C21H24N2O6/c24-19(25)18(23-21(27)29-15-17-10-5-2-6-11-17)12-7-13-22-20(26)28-14-16-8-3-1-4-9-16/h1-6,8-11,18H,7,12-15H2,(H,22,26)(H,23,27)(H,24,25)/t18-/m0/s1 |
N-ALPHA, N-DELTA-BIS(BENZYLOXYCARBONYL)-L-ORNITHINE - Physico-chemical Properties
| Molecular Formula | C21H24N2O6 |
| Molar Mass | 400.43 |
| Density | 1.258 |
| Boling Point | 653.3±55.0 °C(Predicted) |
| Flash Point | 348.9°C |
| Vapor Presure | 5.89E-18mmHg at 25°C |
| pKa | 3.94±0.21(Predicted) |
| Storage Condition | Sealed in dry,2-8°C |
| Refractive Index | 1.574 |
N-ALPHA, N-DELTA-BIS(BENZYLOXYCARBONYL)-L-ORNITHINE - Introduction
N'2,N'5-dibenzyloxycarbonyl-L-ornithine(N'2,N'5-dibenzyloxycarbonyl-L-ornithine) is an organic compound. Its chemical formula is C22H24N2O6.
N'2,N'5-dibenzyloxycarbonyl-L-ornithine is a kind of amino acid protection compounds, commonly used in organic synthesis. Its main use is as a reagent for the temporary protection of amino groups in the synthesis of peptides. It can avoid side reactions in other reactions and protect the stability of the amino group.
The method for preparing N'2,N'5-dibenzyloxycarbonyl-L-ornithine is generally to react benzyloxycarbonyl chloroformate with L-ornithine to form N'2,N'5-dibenzyloxycarbonyl-L-ornithine. The reaction conditions are generally carried out at room temperature.
Regarding safety information, N'2,N'5-dibenzyloxycarbonyl-L-ornithine are less toxic, but it is recommended to wear appropriate protective equipment during use to avoid direct contact with skin, inhalation or ingestion. Care should be taken to avoid contact with strong oxidants and combustibles during storage and handling.
N'2,N'5-dibenzyloxycarbonyl-L-ornithine is a kind of amino acid protection compounds, commonly used in organic synthesis. Its main use is as a reagent for the temporary protection of amino groups in the synthesis of peptides. It can avoid side reactions in other reactions and protect the stability of the amino group.
The method for preparing N'2,N'5-dibenzyloxycarbonyl-L-ornithine is generally to react benzyloxycarbonyl chloroformate with L-ornithine to form N'2,N'5-dibenzyloxycarbonyl-L-ornithine. The reaction conditions are generally carried out at room temperature.
Regarding safety information, N'2,N'5-dibenzyloxycarbonyl-L-ornithine are less toxic, but it is recommended to wear appropriate protective equipment during use to avoid direct contact with skin, inhalation or ingestion. Care should be taken to avoid contact with strong oxidants and combustibles during storage and handling.
Last Update：2024-04-10 22:29:15
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