N-ALPHA-T-BUTOXYCARBONYL-N-DELTA-(2-CHLOROCARBOBENZOXY)-L-ORNITHINE - Names and Identifiers
Name | N(alpha)-boc-N(delta)-(2-chloro-Z)-L-ornithine
|
Synonyms | BocOrn(2-ClZ)-OH BOC-ORN(CL-Z)-OH BOC-ORN(2-CL-Z)-OH Boc-Orn(2-Cl-Z)-OH BOC-L-ORN(2-CLZ)-OH Boc-Orn(2-chloro-Z)-OH BOC-ORN(2-CHLORO-Z)-OH BOC-ORNITHINE(2-CHLORO-Z)-OH BOC-N-DELTA-2-CHLORO-Z-L-ORNITHINE N(alpha)-boc-N(delta)-(2-chloro-Z)-L-ornithine N-ALPHA-T-BUTOXYCARBONYL-N-DELTA-(2-CHLOROCARBOBENZOXY)-L-ORNITHINE N~2~-(tert-butoxycarbonyl)-N~5~-{[(2-chlorobenzyl)oxy]carbonyl}-L-ornithine N-ALPHA-TERT-BUTYLOXYCARBONYL-L-N-DELTA-(2-CHLOROBENZYLOXYCARBONYL)-ORNITHINE
|
CAS | 118554-00-0
|
InChI | InChI=1/C18H25ClN2O6/c1-18(2,3)27-17(25)21-14(15(22)23)9-6-10-20-16(24)26-11-12-7-4-5-8-13(12)19/h4-5,7-8,14H,6,9-11H2,1-3H3,(H,20,24)(H,21,25)(H,22,23)/t14-/m0/s1 |
N-ALPHA-T-BUTOXYCARBONYL-N-DELTA-(2-CHLOROCARBOBENZOXY)-L-ORNITHINE - Physico-chemical Properties
Molecular Formula | C18H25ClN2O6
|
Molar Mass | 400.85 |
Density | 1.256±0.06 g/cm3(Predicted) |
Melting Point | 114-118°C |
Boling Point | 600.7±55.0 °C(Predicted) |
Flash Point | 317.1°C |
Vapor Presure | 2.81E-15mmHg at 25°C |
BRN | 6987223 |
pKa | 3.95±0.21(Predicted) |
Storage Condition | Sealed in dry,2-8°C |
Refractive Index | 1.534 |
N-ALPHA-T-BUTOXYCARBONYL-N-DELTA-(2-CHLOROCARBOBENZOXY)-L-ORNITHINE - Risk and Safety
WGK Germany | 3 |
HS Code | 29242990 |
N-ALPHA-T-BUTOXYCARBONYL-N-DELTA-(2-CHLOROCARBOBENZOXY)-L-ORNITHINE - Introduction
N-tert-Butoxycarbonyl-N'-(2-chlorobenzyloxycarbonyl)-L-ornithine, abbreviated as CBZ-L-ornithine, is an organic compound. Its properties are as follows:
1. Appearance and properties: CBZ-L-ornithine is white or almost white crystalline powder.
2. melting point: about 175-180 degrees Celsius.
3. Solubility: CBZ-L-ornithine can be dissolved in common organic solvents, such as ethanol, methanol and dichloromethane.
The main use of CBZ-L-ornithine is as a protecting group in organic synthesis. It protects the α-amino group in the amino acid from being destroyed during the reaction. In the synthesis of peptides or proteins, CBZ-L-ornithine is often used to protect certain specific amino acids to control the selectivity and yield of the reaction.
The preparation of CBZ-L-ornithine usually starts from L-ornithine, which is first reacted with a tert-butoxycarbonyl compound to obtain N-tert-butoxycarbonyl-L-ornithine, and then reacted with 2-chlorobenzyl alcohol to form CBZ-L-ornithine.
Regarding safety information, CBZ-L-ornithine has not been specifically studied. However, as a chemical, operators should wear appropriate protective equipment, avoid contact with skin and eyes, and ensure that they are used in well-ventilated conditions. If ingested or inhaled, seek medical attention immediately.
Last Update:2024-04-09 20:45:29