163061-73-2
(1R,2R)-(-)-TRANS-1-AMINO-2-INDANOL
CAS: 163061-73-2
Molecular Formula: C9H11NO
163061-73-2 - Names and Identifiers
163061-73-2 - Physico-chemical Properties
| Molecular Formula | C9H11NO |
| Molar Mass | 149.19 |
| Density | 1.212±0.06 g/cm3(Predicted) |
| Melting Point | 142-146°C |
| Boling Point | 290.0±40.0 °C(Predicted) |
| pKa | 14.79±0.40(Predicted) |
| Storage Condition | Keep in dark place,Inert atmosphere,Room temperature |
163061-73-2 - Risk and Safety
| Hazard Symbols | Xi - Irritant |
| Risk Codes | 36/37/38 - Irritating to eyes, respiratory system and skin. |
| Safety Description | S26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice. S36 - Wear suitable protective clothing. |
| WGK Germany | 3 |
163061-73-2 - Introduction
(1R,2R)-(-)-TRANS-1-AMINO-2-INDANOL, also known as (1R,2R)-(-)-TRANS-1-AMINO-2-INDANOL, is an organic compound. Specific properties are as follows:
Nature:
Appearance: Colorless or light yellow solid
Molecular formula: C9H11NO
Molecular weight: 149.19g/mol
Melting point: 76-78 ℃
Boiling point: 315 ℃
Density: 1.19g/cm³
Use:
(1R,2R)-(-)-TRANS-1-AMINO-2-INDANOL is a chiral compound, which is widely used in catalytic reactions in organic synthesis. It can be used as an effective ligand or catalyst to participate in a variety of organic reactions, such as asymmetric catalysis and cyclization reactions. In addition, it is also commonly used in the field of medicine, for the synthesis of a variety of biologically active molecules.
Method:
(1R,2R)-(-)-TRANS-1-AMINO-2-INDANOL can be synthesized by a variety of methods. One commonly used method is by the ammonia alkalization of (1R,2S)-1,2-indenedione. The specific synthesis method can be selected according to the experimental conditions and the desired degree of chirality.
Safety Information:
(1R,2R)-(-)-The use of TRANS-1-AMINO-2-INDANOL should pay attention to the following safety matters:
1. Avoid direct contact with skin and eyes, avoid inhalation or ingestion.
2. Use the process should wear appropriate protective equipment, such as chemical gloves and safety glasses.
3. Operate in a well-ventilated place to avoid dust or vapor.
4. Store away from fire and oxidant, stored in a cool, dry place.
5. If accidental exposure or inhalation, seek medical attention immediately and take appropriate measures according to the doctor's advice.
Please note that the above information is for reference only. Specific experimental operations and safe use should follow relevant laboratory codes and safety regulations.
Nature:
Appearance: Colorless or light yellow solid
Molecular formula: C9H11NO
Molecular weight: 149.19g/mol
Melting point: 76-78 ℃
Boiling point: 315 ℃
Density: 1.19g/cm³
Use:
(1R,2R)-(-)-TRANS-1-AMINO-2-INDANOL is a chiral compound, which is widely used in catalytic reactions in organic synthesis. It can be used as an effective ligand or catalyst to participate in a variety of organic reactions, such as asymmetric catalysis and cyclization reactions. In addition, it is also commonly used in the field of medicine, for the synthesis of a variety of biologically active molecules.
Method:
(1R,2R)-(-)-TRANS-1-AMINO-2-INDANOL can be synthesized by a variety of methods. One commonly used method is by the ammonia alkalization of (1R,2S)-1,2-indenedione. The specific synthesis method can be selected according to the experimental conditions and the desired degree of chirality.
Safety Information:
(1R,2R)-(-)-The use of TRANS-1-AMINO-2-INDANOL should pay attention to the following safety matters:
1. Avoid direct contact with skin and eyes, avoid inhalation or ingestion.
2. Use the process should wear appropriate protective equipment, such as chemical gloves and safety glasses.
3. Operate in a well-ventilated place to avoid dust or vapor.
4. Store away from fire and oxidant, stored in a cool, dry place.
5. If accidental exposure or inhalation, seek medical attention immediately and take appropriate measures according to the doctor's advice.
Please note that the above information is for reference only. Specific experimental operations and safe use should follow relevant laboratory codes and safety regulations.
Last Update：2024-04-09 15:18:03
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