(S)-1-{-2-[DI(1-NAPHTHYL)PHOSPHINO]FERROCENYL}ETHYLDI(3,5-XYLYL)PHOSPHINE
(S)-1-{(R)-2-[DI(1-NAPHTHYL)PHOSPHINO]FERROCENYL}ETHYLDI(3,5-XYLYL)PHOSPHINE
CAS: 851308-41-3
Molecular Formula: C50H49FeP2
(S)-1-{-2-[DI(1-NAPHTHYL)PHOSPHINO]FERROCENYL}ETHYLDI(3,5-XYLYL)PHOSPHINE - Names and Identifiers
(S)-1-{-2-[DI(1-NAPHTHYL)PHOSPHINO]FERROCENYL}ETHYLDI(3,5-XYLYL)PHOSPHINE - Physico-chemical Properties
| Molecular Formula | C50H49FeP2 |
| Molar Mass | 767.716582 |
| Storage Condition | under inert gas (nitrogen or Argon) at 2-8°C |
(S)-1-{-2-[DI(1-NAPHTHYL)PHOSPHINO]FERROCENYL}ETHYLDI(3,5-XYLYL)PHOSPHINE - Risk and Safety
| WGK Germany | 3 |
| HS Code | 29319090 |
(S)-1-{-2-[DI(1-NAPHTHYL)PHOSPHINO]FERROCENYL}ETHYLDI(3,5-XYLYL)PHOSPHINE - Introduction
(S)-1-{(R)-2-[DI(1-NAPHTHYL)PHOSPHINO]FERROCENYL}ETHYLDI(3,5-XYLYL)PHOSPHINE is an organic compound. Its molecular formula is C52H48FeNP2 and its molecular weight is 775.15g/mol. It is a chiral compound consisting of di (1-naphthyl) phosphine and ferrocenyl attached to ethyldi (3,5-xylyl) phosphine.
This compound can be used as a chiral catalyst and has important applications in organic synthesis. It can catalyze the asymmetric hydrogenation reaction, asymmetric Michael addition reaction, Knoevenagel condensation reaction and other organic reactions. Its chiral structure allows it to selectively control the chirality of the product of the reaction.
(S)-1-{(R)-2-[DI(1-NAPHTHYL)PHOSPHINO]FERROCENYL}ETHYLDI(3,5-XYLYL)PHOSPHINE can be prepared by attaching di (1-naphthyl) phosphine and ferrocenyl to ethyldi (3,5-xylyl) phosphine. The particular synthetic method may be selected on a case-by-case basis, but generally includes selective substitution and reaction formation.
Regarding safety information, the use of organic compounds should be carried out in accordance with relevant laboratory operating procedures, including wearing personal protective equipment necessary for chemical laboratories and paying attention to safety measures during experimental operations. At the same time, for this compound, must be properly stored, avoid contact with fire, to prevent its reaction with oxygen, moisture and halogen. During use, care should be taken to prevent inhalation or contact with skin and eyes. It is recommended to operate in a specialized chemical laboratory and follow the relevant safe operating procedures.
This compound can be used as a chiral catalyst and has important applications in organic synthesis. It can catalyze the asymmetric hydrogenation reaction, asymmetric Michael addition reaction, Knoevenagel condensation reaction and other organic reactions. Its chiral structure allows it to selectively control the chirality of the product of the reaction.
(S)-1-{(R)-2-[DI(1-NAPHTHYL)PHOSPHINO]FERROCENYL}ETHYLDI(3,5-XYLYL)PHOSPHINE can be prepared by attaching di (1-naphthyl) phosphine and ferrocenyl to ethyldi (3,5-xylyl) phosphine. The particular synthetic method may be selected on a case-by-case basis, but generally includes selective substitution and reaction formation.
Regarding safety information, the use of organic compounds should be carried out in accordance with relevant laboratory operating procedures, including wearing personal protective equipment necessary for chemical laboratories and paying attention to safety measures during experimental operations. At the same time, for this compound, must be properly stored, avoid contact with fire, to prevent its reaction with oxygen, moisture and halogen. During use, care should be taken to prevent inhalation or contact with skin and eyes. It is recommended to operate in a specialized chemical laboratory and follow the relevant safe operating procedures.
Last Update：2024-04-10 22:29:15
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Product Name: (S)-1-{(RP)-2-[Di(1-naphthyl)phosphino]ferrocenyl}ethyldi(3,5-xylyl)phosphine Visit Supplier Webpage Request for quotationCAS: 851308-41-3
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