FMOC-L-2-PYRIDYLALANINE
(S)-N-FMOC-(2-Pyridyl)alanine
CAS: 185379-40-2
Molecular Formula: C23H20N2O4
FMOC-L-2-PYRIDYLALANINE - Names and Identifiers
| Name | (S)-N-FMOC-(2-Pyridyl)alanine |
| Synonyms | Fmoc-2-Pal-OH FMOC-ALA(2-PYRI)-OH FMOC-2'-PYRIDYL-L-ALA FMOC-ALA(2-PYRIDYL)-OH FMOC-ALA(2'-PYRIDYL)-OH Fmoc-L-2-Pyridylalanine FMOC-L-2-PYRIDYLALANINE FMOC-Β-(2-PYRIDYL)-ALA-OH Fmoc-3-(2-Pyridyl)-L-alanine Fmoc-L-3-(2-Pyridyl)-alanine FMOC-3-(2-PYRIDYL)-L-ALANINE (S)-N-FMOC-(2-Pyridyl)alanine FMOC-3-(2'-PYRIDYL)-L-ALANINE FMOC-(S)-2-AMINO-3-(2'-PYRIDYL)PROPANOIC ACID |
| CAS | 185379-40-2 |
| InChI | InChI=1/C23H20N2O4/c26-22(27)21(13-15-7-5-6-12-24-15)25-23(28)29-14-20-18-10-3-1-8-16(18)17-9-2-4-11-19(17)20/h1-12,20-21H,13-14H2,(H,25,28)(H,26,27)/p-1/t21-/m0/s1 |
| InChIKey | DXIVJCDZOMUITR-NRFANRHFSA-N |
FMOC-L-2-PYRIDYLALANINE - Physico-chemical Properties
| Molecular Formula | C23H20N2O4 |
| Molar Mass | 388.42 |
| Density | 1.2692 (rough estimate) |
| Melting Point | 151 °C |
| Boling Point | 514.13°C (rough estimate) |
| Flash Point | 335.4°C |
| Solubility | Dichloromethane (Sparingly), Dimethylformamide (Slightly, Sonicated), DMSO (Slig |
| Vapor Presure | 8.74E-17mmHg at 25°C |
| Appearance | White powder |
| Color | Pale brown |
| pKa | 2.98±0.10(Predicted) |
| Storage Condition | 2-8°C |
| Refractive Index | 1.6300 (estimate) |
| MDL | MFCD00672564 |
FMOC-L-2-PYRIDYLALANINE - Risk and Safety
| Hazard Symbols | Xi - Irritant |
| Safety Description | S22 - Do not breathe dust. S36 - Wear suitable protective clothing. |
| WGK Germany | 3 |
| HS Code | 29223900 |
| Hazard Class | IRRITANT |
FMOC-L-2-PYRIDYLALANINE - Introduction
(S)-N-FMOC-(2-pyriridyl) alanine is an amino acid derivative with the following properties:
1. Appearance:(S)-N-FMOC-(2-Pyridyl)alanine is white to off-white crystal or powder.
2. Stability: It has good stability at room temperature.
3. Solubility:(S)-N-FMOC-(2-pyriridyl) alanine is soluble in some organic solvents (such as dimethyl sulfoxide, dichloromethane, etc.).
(S)-N-FMOC-(2-Pyridyl)alanine uses mainly include:
1. Biochemical research: It is often used as a raw material for the synthesis of polypeptides and peptide compounds for the synthesis of more complex biologically active molecules.
2. Drug Research:(S)-N-FMOC-(2-pyriridyl) alanine has a wide range of applications in drug research, for the synthesis of peptide drugs and peptide analogs.
3. Anti-Tumor Research: It is also used to research and develop compounds with anti-tumor activity and inhibit the proliferation of cancer cells.
(S)-N-FMOC-(2-pyriridyl) alanine is generally produced by chemical synthesis. A particular preparation will involve a series of organic synthesis steps, requiring suitable reagents and conditions.
Regarding safety information, the following items should be paid attention to during operation:
1. Avoid inhaling the odor and vapor of the powder or solution, and use a protective mask and gloves for operation.
2. Avoid contact with skin and eyes. If there is contact, rinse with plenty of water immediately and seek medical help.
3. Storage should be kept dry and sealed, away from the fire and oxidant.
Please note that the above information is for reference only, and the specific information and operation details should be determined and operated according to the actual situation and relevant literature.
1. Appearance:(S)-N-FMOC-(2-Pyridyl)alanine is white to off-white crystal or powder.
2. Stability: It has good stability at room temperature.
3. Solubility:(S)-N-FMOC-(2-pyriridyl) alanine is soluble in some organic solvents (such as dimethyl sulfoxide, dichloromethane, etc.).
(S)-N-FMOC-(2-Pyridyl)alanine uses mainly include:
1. Biochemical research: It is often used as a raw material for the synthesis of polypeptides and peptide compounds for the synthesis of more complex biologically active molecules.
2. Drug Research:(S)-N-FMOC-(2-pyriridyl) alanine has a wide range of applications in drug research, for the synthesis of peptide drugs and peptide analogs.
3. Anti-Tumor Research: It is also used to research and develop compounds with anti-tumor activity and inhibit the proliferation of cancer cells.
(S)-N-FMOC-(2-pyriridyl) alanine is generally produced by chemical synthesis. A particular preparation will involve a series of organic synthesis steps, requiring suitable reagents and conditions.
Regarding safety information, the following items should be paid attention to during operation:
1. Avoid inhaling the odor and vapor of the powder or solution, and use a protective mask and gloves for operation.
2. Avoid contact with skin and eyes. If there is contact, rinse with plenty of water immediately and seek medical help.
3. Storage should be kept dry and sealed, away from the fire and oxidant.
Please note that the above information is for reference only, and the specific information and operation details should be determined and operated according to the actual situation and relevant literature.
Last Update：2024-04-09 20:02:46
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View History
FMOC-L-2-PYRIDYLALANINE
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