Ndelta-Benzyloxycarbonyl-Nalpha-Boc-L-ornithine
N(alpha)-boc-N(delta)-Z-L-ornithine
CAS: 2480-93-5
Molecular Formula: C18H26N2O6
Ndelta-Benzyloxycarbonyl-Nalpha-Boc-L-ornithine - Names and Identifiers
| Name | N(alpha)-boc-N(delta)-Z-L-ornithine |
| Synonyms | Z-Orn(Boc) BOC-Orn(Z)-OH BOC-L-ORN(BZL)-OH na-T-boc-N-delta-cbz-L-ornithine N(alpha)-boc-N(delta)-Z-L-ornithine Ndelta-Benzyloxycarbonyl-Nalpha-Boc-L-ornithine N-tert-Butoxycarbonyl-N'-benzyloxycarbonyl-L-ornithine N~5~-[(benzyloxy)carbonyl]-N~2~-(tert-butoxycarbonyl)ornithine N~5~-[(benzyloxy)carbonyl]-N~2~-(tert-butoxycarbonyl)-L-ornithine (S)-5-(((Benzyloxy)carbonyl)aMino)-2-((tert-butoxycarbonyl)aMino)pentanoic acid (2S)-2-[(2-methylpropan-2-yl)oxycarbonylamino]-5-(phenylmethoxycarbonylamino)pentanoic acid |
| CAS | 2480-93-5 |
| InChI | InChI=1/C18H26N2O6/c1-18(2,3)26-17(24)20-14(15(21)22)10-7-11-19-16(23)25-12-13-8-5-4-6-9-13/h4-6,8-9,14H,7,10-12H2,1-3H3,(H,19,23)(H,20,24)(H,21,22)/t14-/m0/s1 |
Ndelta-Benzyloxycarbonyl-Nalpha-Boc-L-ornithine - Physico-chemical Properties
| Molecular Formula | C18H26N2O6 |
| Molar Mass | 366.41 |
| Density | 1.193±0.06 g/cm3(Predicted) |
| Melting Point | 92.0 to 95.0 °C |
| Boling Point | 579.1±50.0 °C(Predicted) |
| Flash Point | 304°C |
| Solubility | almost transparency in Methanol |
| Vapor Presure | 2.99E-14mmHg at 25°C |
| Appearance | White to off-white powder |
| Color | White to Almost white |
| BRN | 2783761 |
| pKa | 3.96±0.21(Predicted) |
| Storage Condition | Sealed in dry,Room Temperature |
| Refractive Index | 1.526 |
| MDL | MFCD00038259 |
Ndelta-Benzyloxycarbonyl-Nalpha-Boc-L-ornithine - Risk and Safety
| Safety Description | 24/25 - Avoid contact with skin and eyes. |
| WGK Germany | 3 |
| HS Code | 2924 29 70 |
| Hazard Class | IRRITANT |
Ndelta-Benzyloxycarbonyl-Nalpha-Boc-L-ornithine - Introduction
N(alpha)-boc-N(delta)-Z-L-ornithine(N(alpha)-boc-N(delta)-Z-L-ornithine) is an amino acid derivative. It has the following characteristics:
1. Appearance: usually white to light yellow powder substance.
2. Solubility: slightly soluble in water and some organic solvents, such as methanol and dimethyl sulfoxide.
3. Stability: It is relatively stable under regular experimental conditions, but should avoid long-term exposure to high temperature and high humidity.
N(alpha)-boc-N(delta)-Z-L-ornithine is commonly used in organic synthetic chemistry. It can be used as an intermediate and protecting group for peptide synthesis. It is usually used to synthesize polypeptide molecules with special chemical properties and biological activities. It can also be used to study ornithine metabolic pathways and the properties and mechanisms of action of related enzymes.
The method for preparing N(alpha)-boc-N(delta)-Z-L-ornithine is as follows: usually using N-t-butoxycarbonyl-L-ornithine as a raw material, it is first treated in the presence of sodium hydroxide to form N-amino ornithine, which is then reacted with benzylchlorochloride to produce the target compound.
Regarding safety information, N(alpha)-boc-N(delta)-Z-L-ornithine are generally considered to be relatively safe under normal operating conditions. However, it is still necessary to comply with laboratory safety practices, such as wearing personal protective equipment, avoiding direct contact with skin and eyes, and ensuring that the operating area is well ventilated. If ingested or inhaled, seek medical attention immediately.
1. Appearance: usually white to light yellow powder substance.
2. Solubility: slightly soluble in water and some organic solvents, such as methanol and dimethyl sulfoxide.
3. Stability: It is relatively stable under regular experimental conditions, but should avoid long-term exposure to high temperature and high humidity.
N(alpha)-boc-N(delta)-Z-L-ornithine is commonly used in organic synthetic chemistry. It can be used as an intermediate and protecting group for peptide synthesis. It is usually used to synthesize polypeptide molecules with special chemical properties and biological activities. It can also be used to study ornithine metabolic pathways and the properties and mechanisms of action of related enzymes.
The method for preparing N(alpha)-boc-N(delta)-Z-L-ornithine is as follows: usually using N-t-butoxycarbonyl-L-ornithine as a raw material, it is first treated in the presence of sodium hydroxide to form N-amino ornithine, which is then reacted with benzylchlorochloride to produce the target compound.
Regarding safety information, N(alpha)-boc-N(delta)-Z-L-ornithine are generally considered to be relatively safe under normal operating conditions. However, it is still necessary to comply with laboratory safety practices, such as wearing personal protective equipment, avoiding direct contact with skin and eyes, and ensuring that the operating area is well ventilated. If ingested or inhaled, seek medical attention immediately.
Last Update：2024-04-09 20:02:46
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CAS: 2480-93-5
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