N-α-Boc-N-δ-allyloxycarbonyl-L-ornithine
Fmoc-Orn(Aloc)-OH
CAS: 147290-11-7
Molecular Formula: C24H26N2O6
N-α-Boc-N-δ-allyloxycarbonyl-L-ornithine - Names and Identifiers
| Name | Fmoc-Orn(Aloc)-OH |
| Synonyms | Fmoc-Orn(Aloc)-OH FMOC-ORN(ALOC)-OH Fmoc-Orn(Alloc)-OH FMOC-L-ORN(ALLOC)-OH nα-fmoc-nδ-alloc-l-ornithine Nδ-Alloc-Nα-Fmoc-L-ornithine N-α-Boc-N-δ-allyloxycarbonyl-L-ornithine Nα-Fmoc-Nδ-Alloc-L-ornithine, Nδ-Alloc-Nα-Fmoc-L-ornithine N2-(9-Fluorenylmethyloxycarbonyl)-N5-allyloxycarbonyl-L-ornithine NDELTA-Allyloxycarbonyl-NALPHA-9-fluorenylmethoxycarbonyl-L-ornithine N-ALPHA-(9-FLUOROENYLMETHYLOXYCARBONYL)-N--ALLYLOXYCARBONYL-L-ORNITHINE N~2~-[(9H-fluoren-9-ylmethoxy)carbonyl]-N~5~-[(prop-2-en-1-yloxy)carbonyl]-L-ornithine |
| CAS | 147290-11-7 |
| InChI | InChI=1/C24H26N2O6/c1-2-14-31-23(29)25-13-7-12-21(22(27)28)26-24(30)32-15-20-18-10-5-3-8-16(18)17-9-4-6-11-19(17)20/h2-6,8-11,20-21H,1,7,12-15H2,(H,25,29)(H,26,30)(H,27,28)/t21-/m0/s1 |
N-α-Boc-N-δ-allyloxycarbonyl-L-ornithine - Physico-chemical Properties
| Molecular Formula | C24H26N2O6 |
| Molar Mass | 438.47 |
| Density | 1?+-.0.06 g/cm3(Predicted) |
| Boling Point | 683.9±55.0 °C(Predicted) |
| Flash Point | 367.4°C |
| Vapor Presure | 1.21E-19mmHg at 25°C |
| Appearance | Solid |
| pKa | 3.85±0.21(Predicted) |
| Storage Condition | Sealed in dry,Store in freezer, under -20°C |
| Refractive Index | 1.583 |
N-α-Boc-N-δ-allyloxycarbonyl-L-ornithine - Risk and Safety
| WGK Germany | 3 |
| HS Code | 29225090 |
N-α-Boc-N-δ-allyloxycarbonyl-L-ornithine - Introduction
Fmoc-Orn(Aloc)-OH is a compound that has the following properties:
1. Appearance: usually white or white solid.
2. Solubility: It has good solubility in organic solvents, such as dichloromethane, dimethylformamide, etc.
3. Stability: relatively stable, but should avoid light, high temperature and humidity and other effects.
Fmoc-Orn(Aloc)-OH is mainly used in the fields of biochemistry and organic synthesis and has the following uses:
1. Peptide synthesis: As an amino acid protecting group, it can be used to synthesize peptide chains with specific peptide sequences and structures.
2. Drug research: as a component or intermediate of drug molecules, it participates in the synthesis and research of drugs.
The method of preparing Fmoc-Orn(Aloc)-OH includes the following steps:
1. First, n5-allyloxycarbonyl-l-ornithine is synthesized, which is usually achieved by removing the protecting Group of the amino acid and removing the protecting Group of the carboxyl group.
2. Then, an Fmoc (9-fluoroalkylcarbonyl) group was introduced into n5-allyloxycarbonyl-1-ornithine to give the target compound Fmoc-Orn(Aloc)-OH.
For safety information, specific safety data for Fmoc-Orn(Aloc)-OH should refer specifically to the chemical's safety data sheet (MSDS). During handling and handling, laboratory safety procedures should be followed and appropriate personal protective measures should be taken, such as wearing protective glasses and gloves. For any chemical, avoid prolonged or heavy exposure and try to operate in a well-ventilated area. In case of accident or discomfort, seek medical help immediately.
1. Appearance: usually white or white solid.
2. Solubility: It has good solubility in organic solvents, such as dichloromethane, dimethylformamide, etc.
3. Stability: relatively stable, but should avoid light, high temperature and humidity and other effects.
Fmoc-Orn(Aloc)-OH is mainly used in the fields of biochemistry and organic synthesis and has the following uses:
1. Peptide synthesis: As an amino acid protecting group, it can be used to synthesize peptide chains with specific peptide sequences and structures.
2. Drug research: as a component or intermediate of drug molecules, it participates in the synthesis and research of drugs.
The method of preparing Fmoc-Orn(Aloc)-OH includes the following steps:
1. First, n5-allyloxycarbonyl-l-ornithine is synthesized, which is usually achieved by removing the protecting Group of the amino acid and removing the protecting Group of the carboxyl group.
2. Then, an Fmoc (9-fluoroalkylcarbonyl) group was introduced into n5-allyloxycarbonyl-1-ornithine to give the target compound Fmoc-Orn(Aloc)-OH.
For safety information, specific safety data for Fmoc-Orn(Aloc)-OH should refer specifically to the chemical's safety data sheet (MSDS). During handling and handling, laboratory safety procedures should be followed and appropriate personal protective measures should be taken, such as wearing protective glasses and gloves. For any chemical, avoid prolonged or heavy exposure and try to operate in a well-ventilated area. In case of accident or discomfort, seek medical help immediately.
Last Update：2024-04-09 21:01:54
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CAS: 147290-11-7
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CAS: 147290-11-7
Tel: 18301782025
Email: 3008007409@qq.com
Mobile: 18021002903
QQ: 3008007409
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