158807-47-7
(R)-N-Boc-3-Amino-3-Phenyl-Propan-1-Ol
CAS: 158807-47-7
Molecular Formula: C14H21NO3
158807-47-7 - Names and Identifiers
158807-47-7 - Physico-chemical Properties
| Molecular Formula | C14H21NO3 |
| Molar Mass | 251.32 |
| Density | 1.083±0.06 g/cm3(Predicted) |
| Boling Point | 404.6±38.0 °C(Predicted) |
| Appearance | White powder |
| pKa | 11.77±0.46(Predicted) |
| Storage Condition | 2-8°C |
158807-47-7 - Risk and Safety
| Safety Description | 24/25 - Avoid contact with skin and eyes. |
| HS Code | 29221990 |
| Hazard Class | IRRITANT |
158807-47-7 - Introduction
(R)-N-Boc-3-Amino-3-Phenyl-Propan-1-Ol is an organic compound with the following properties:
1. Appearance: Colorless or light yellow crystalline solid.
2. Molecular formula: C16H23NO3.
3. Molecular weight: 277.36g/mol.
4. Melting Point: About 75-78 ℃.
5. Solubility: Good solubility in common organic solvents.
(R)-N-Boc-3-Amino-3-Phenyl-Propan-1-Ol is a chiral compound, which can be used as a chiral inducer or catalyst in organic synthesis. This compound is often used as a catalyst in asymmetric synthesis reactions, especially in the preparation of chiral drugs and bioactive molecules.
This compound can be prepared by the following method: reacting silver benzyl chloride with N-tert-butoxycarbonyl-L-demethoxymalate, and then reducing the obtained intermediate, chiral purification was finally performed.
Regarding safety information, due to differences in the specific application and use conditions of the compound, it is recommended to refer to the relevant chemical Safety Data Sheet (MSDS) or perform reasonable safety operations before use.
1. Appearance: Colorless or light yellow crystalline solid.
2. Molecular formula: C16H23NO3.
3. Molecular weight: 277.36g/mol.
4. Melting Point: About 75-78 ℃.
5. Solubility: Good solubility in common organic solvents.
(R)-N-Boc-3-Amino-3-Phenyl-Propan-1-Ol is a chiral compound, which can be used as a chiral inducer or catalyst in organic synthesis. This compound is often used as a catalyst in asymmetric synthesis reactions, especially in the preparation of chiral drugs and bioactive molecules.
This compound can be prepared by the following method: reacting silver benzyl chloride with N-tert-butoxycarbonyl-L-demethoxymalate, and then reducing the obtained intermediate, chiral purification was finally performed.
Regarding safety information, due to differences in the specific application and use conditions of the compound, it is recommended to refer to the relevant chemical Safety Data Sheet (MSDS) or perform reasonable safety operations before use.
Last Update：2024-04-09 15:17:53
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View History
158807-47-7
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