s-3,5me-4meoph-tbu - Names and Identifiers
s-3,5me-4meoph-tbu - Physico-chemical Properties
Molecular Formula | C38H46FeO2P2
|
Molar Mass | 652.58 |
Storage Condition | under inert gas (nitrogen or Argon) at 2-8°C |
s-3,5me-4meoph-tbu - Risk and Safety
WGK Germany | 3 |
HS Code | 29319090 |
s-3,5me-4meoph-tbu - Introduction
(2S)-1-[(1S)-1-[BIS(1,1-DIMETHYLETHYL)PHOSPHINO]ETHYL]-2-[BIS(4-METHOXY-3,5-DIMETHYLPHENYL)PHOSPHINO]FERROCENE (((2S)-1-[(1S)-1-[BIS (1,1-DIMETHYY] -3-PHOSPHINO), 5-DIMETHYLPHENYL)PHOSPHINO]FERROCENE) is a chiral organic compound.
Nature:
-Appearance: solid, usually orange crystals.
-Molecular formula: C70H80FeP3O2
-Molecular weight: 1050.78g/mol
-Melting point: 176-178 degrees Celsius
-Soluble in some organic solvents, such as chloroform, dimethylformamide and benzene.
Use:
- (2S)-1-[(1S)-1-[BIS(1,1-DIMETHYLETHYL)PHOSPHINO]ETHYL]-2-[BIS(4-METHOXY-3,5-DIMETHYLPHENYL)PHOSPHINO]FERROCENE can be used as chiral ligands in organic synthesis reactions. It can form complexes with copper, palladium, rhodium and other metals, and is used in catalytic reactions, such as asymmetric hydrogenation, asymmetric rearrangement and asymmetric oxidation.
Preparation Method:
The preparation method of- (2S)-1-[(1S)-1-[BIS(1,1-DIMETHYLETHYL)PHOSPHINO]ETHYL]-2-[BIS(4-METHOXY-3,5-DIMETHYLPHENYL)PHOSPHINO]FERROCENE is complicated and requires multi-step reaction.
-A common preparation method is to introduce phosphorus ligands and methoxy substituents through a multi-step reaction starting from ferrocene.
Safety Information:
- (2S)-1-[(1S)-1-[BIS(1,1-DIMETHYLETHYL)PHOSPHINO]ETHYL]-2-[BIS(4-METHOXY-3,5-DIMETHYLPHENYL)PHOSPHINO]FERROCENE has high safety, but as an organic compound, it still needs to comply with general chemical laboratory safety procedures.
-Avoid inhaling dust or skin contact. If you come into contact with skin or eyes, rinse with plenty of water in time.
-Keep dry during storage and avoid contact with harmful substances such as oxygen and moisture to prevent unnecessary reactions.
Last Update:2024-04-10 22:29:15