(S)-1-{(S)-2-[Di(2-furyl)phosphino]ferrocenyl}ethylbis(2-methylphenyl)phosphine - Names and Identifiers
(S)-1-{(S)-2-[Di(2-furyl)phosphino]ferrocenyl}ethylbis(2-methylphenyl)phosphine - Physico-chemical Properties
Molecular Formula | C34H26FeO2P2
|
Molar Mass | 584.37 |
Storage Condition | under inert gas (nitrogen or Argon) at 2-8°C |
(S)-1-{(S)-2-[Di(2-furyl)phosphino]ferrocenyl}ethylbis(2-methylphenyl)phosphine - Risk and Safety
WGK Germany | 3 |
HS Code | 29321900 |
(S)-1-{(S)-2-[Di(2-furyl)phosphino]ferrocenyl}ethylbis(2-methylphenyl)phosphine - Introduction
(2S)-1-[(1S)-1-[BIS(2-METHYLPHENYL)PHOSPHINO]ETHYL]-2-(DI-2-FURANYLPHOSPHINO)FERROCENE is a chiral organic compound. The following is an introduction to its nature, use, preparation and safety information:
Nature:
-Appearance: Colorless or light yellow solid.
-Melting point: about 180-190 ℃.
-Solubility: Soluble in some common organic solvents.
Use:
-Catalyst: This compound is a chiral ligand, widely used in metal-catalyzed reactions. It exhibits high catalytic activity and selectivity in asymmetric catalytic reactions, including asymmetric hydrogenation, reduction, asymmetric cyclization and asymmetric carbonylation.
Preparation Method:
-A commonly used preparation method is to synthesize through a two-step reaction: first, (2-furyl) phosphine chloride and (dimethyl sulfoxide) ferrocenyldiethylphosphine bromide are reacted with dimethyl sulfoxide to generate (RP)-2-[di (2-furyl) phosphino] ferrocenyl compound; then, reaction with bis (dimethylaminoethyl) diphenylphosphine under basic conditions yields the final target compound.
Safety Information:
-This compound has limited safety information, but it is generally believed to have low toxicity to the human body.
-Nevertheless, any chemical should be handled with caution and in accordance with appropriate laboratory practices and safe operating procedures.
-When using and handling this compound, care should be taken to avoid contact with skin and eyes and maintain good ventilation.
Last Update:2024-04-09 21:01:54