1237588-12-3
N-[2-(di-1-adamantylphosphino)phenyl]morpholine
CAS: 1237588-12-3
Molecular Formula: C30H42NOP
1237588-12-3 - Names and Identifiers
1237588-12-3 - Physico-chemical Properties
| Molecular Formula | C30H42NOP |
| Molar Mass | 463.63 |
| Melting Point | 219-224°C |
| Appearance | crystal |
| Color | white to yellow |
| pKa | 4.75±0.40(Predicted) |
| Storage Condition | 2-8°C |
| Sensitive | air sensitive |
1237588-12-3 - Risk and Safety
| Hazard Symbols | Xi - Irritant |
| Risk Codes | 36/37/38 - Irritating to eyes, respiratory system and skin. |
| Safety Description | 26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice. |
| WGK Germany | 3 |
1237588-12-3 - Introduction
N-[2-(di-1-adamantylphosphino)phenyl]morpholine is an organic compound with a chemical formula of C27H36NOP and a relative molecular mass of 421.56g/mol. It is a liquid, colorless to light yellow at room temperature.
The main use of this compound is as a catalyst for ligands and catalysts. It can form stable complexes with transition metals and can be used in organic synthesis reactions. As an organic catalyst, it can be used in asymmetric catalytic reactions, such as asymmetric hydrogenation and asymmetric nucleophilic substitution reactions. In addition, it can also be used in chemical fields such as the synthesis of organometallic compounds and organophosphorus compounds.
N-[2-(di-1-adamantylphosphino)phenyl]morpholine are generally prepared by reacting 2-bromotoluene and dibromoadamantane, and then reacting with morpholine under basic conditions to produce the desired product. The preparation process requires attention to operating conditions and safety measures when handling hazardous chemicals.
When using N-[2-(di-1-adamantylphosphino)phenyl]morpholine, safety practices should be followed. It is an organic compound that is irritating to the skin and eyes and is potentially toxic. Therefore, wear appropriate personal protective equipment, such as laboratory gloves and goggles, and avoid direct contact during operation. At the same time, it should be used in a well-ventilated laboratory environment to avoid inhaling its vapors. If an accident occurs, immediately flush the affected area with plenty of water and seek medical help.
The main use of this compound is as a catalyst for ligands and catalysts. It can form stable complexes with transition metals and can be used in organic synthesis reactions. As an organic catalyst, it can be used in asymmetric catalytic reactions, such as asymmetric hydrogenation and asymmetric nucleophilic substitution reactions. In addition, it can also be used in chemical fields such as the synthesis of organometallic compounds and organophosphorus compounds.
N-[2-(di-1-adamantylphosphino)phenyl]morpholine are generally prepared by reacting 2-bromotoluene and dibromoadamantane, and then reacting with morpholine under basic conditions to produce the desired product. The preparation process requires attention to operating conditions and safety measures when handling hazardous chemicals.
When using N-[2-(di-1-adamantylphosphino)phenyl]morpholine, safety practices should be followed. It is an organic compound that is irritating to the skin and eyes and is potentially toxic. Therefore, wear appropriate personal protective equipment, such as laboratory gloves and goggles, and avoid direct contact during operation. At the same time, it should be used in a well-ventilated laboratory environment to avoid inhaling its vapors. If an accident occurs, immediately flush the affected area with plenty of water and seek medical help.
Last Update：2024-04-10 22:29:15
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Email: r@reformchem.com
Mobile: +86-17551318830
QQ: 3785839865
Product Name: N-[2-(di-1-adamantylphosphino) phenyl]morpholine Visit Supplier Webpage Request for quotation
CAS: 1237588-12-3
Tel: 18301782025
Email: 3008007409@qq.com
Mobile: 18021002903
QQ: 3008007409
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CAS: 1237588-12-3
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QQ: 3008007409
Wechat: 18301782025
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Product Name: N-[2-(di-1-adamantylphosphino)phenyl]morpholine Request for quotationCAS: 1237588-12-3
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Email: biz5@infsci.com
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