268220-91-3

Basic information

• Product Name: (S)-1-[(1R)-2-(DIPHENYLPHOSPHINO)FERROCENYL]ETHYLDI-TERT-BUTYLPHOSPHINE
• Synonyms: JOSIPHOS SL-J002-2;(+)-1,1'-BIS[(2R,4R)-2,4-DIETHYLPHOSPHONATO]FERROCENE;(+)-1,1'-BIS((2R,4R)-2,4-DIETHYLPHOSPHOTANO)FERROCENE;(S,S)-1-[1-(DI-TERT-BUTYLPHOSPHINO)ETHYL]-2-(DIPHENYLPHOSPHINO)FERROCENE;(S)-1-[(1R)-2-(DIPHENYLPHOSPHINO)FERROCENYL]ETHYLDI-TERT-BUTYLPHOSPHINE;(R,R)-ET-FERROTANE(TM);(S)-(+)-1-[(R)-2-(DIPHENYLPHOSPHINO)FERROCENYL]ETHYLDI-T-BUTYLPHOSPHINE;(+)-1,1'-Bis((2R,4R)-2,4-diethylphosphotano)ferrocene,min.95%(R,R)-Et-FerroTANE
• CAS NO: 268220-91-3
• Molecular Formula: 2C12H18P.Fe
• Molecular Weight: 442.34
• Mol File: 268220-91-3.mol
• Article Data: 0

Chemical Properties

• Melting Point: 76°C
• Appearance: /
• CAS DataBase Reference: (S)-1-[(1R)-2-(DIPHENYLPHOSPHINO)FERROCENYL]ETHYLDI-TERT-BUTYLPHOSPHINE(CAS DataBase Reference)
• NIST Chemistry Reference: (S)-1-[(1R)-2-(DIPHENYLPHOSPHINO)FERROCENYL]ETHYLDI-TERT-BUTYLPHOSPHINE(268220-91-3)
• EPA Substance Registry System: (S)-1-[(1R)-2-(DIPHENYLPHOSPHINO)FERROCENYL]ETHYLDI-TERT-BUTYLPHOSPHINE(268220-91-3)

Safety Data

• Statements: 36/37/38
• Safety Statements: 26-36/37/39
• WGK Germany: 3
• F: 10
• Hazardous Substances Data: 268220-91-3(Hazardous Substances Data)

Usage

Description

(S)-1-[(1R)-2-(DIPHENYLPHOSPHINO)FERROCENYL]ETHYLDI-TERT-BUTYLPHOSPHINE is a complex chemical compound that features a ferrocene moiety, diphenylphosphino groups, and tert-butylphosphine groups. It possesses a chiral center and is stereochemically defined as (S)-1-[(1R)-2-(diphenylphosphino)ferrocenyl]ethyldi-tert-butylphosphine. (S)-1-[(1R)-2-(DIPHENYLPHOSPHINO)FERROCENYL]ETHYLDI-TERT-BUTYLPHOSPHINE is recognized for its utility in organometallic chemistry and asymmetric catalysis reactions, where its structure and chirality contribute to promoting enantioselective transformations, such as asymmetric hydrogenation reactions. The ferrocene component endows the compound with stability and facilitates coordination with transition metals for various catalytic processes. In essence, (S)-1-[(1R)-2-(DIPHENYLPHOSPHINO)FERROCENYL]ETHYLDI-TERT-BUTYLPHOSPHINE is a multifaceted and significant chemical entity in the realm of organic chemistry and catalysis.

Uses

Used in Organometallic Chemistry:
(S)-1-[(1R)-2-(DIPHENYLPHOSPHINO)FERROCENYL]ETHYLDI-TERT-BUTYLPHOSPHINE is utilized as a ligand for its ability to bind with transition metals, enhancing the stability and reactivity of organometallic complexes.
Used in Asymmetric Catalysis:
In the field of asymmetric catalysis, (S)-1-[(1R)-2-(DIPHENYLPHOSPHINO)FERROCENYL]ETHYLDI-TERT-BUTYLPHOSPHINE is employed as a chiral ligand to promote enantioselective transformations, which are crucial for producing enantiomerically pure compounds essential in pharmaceuticals and agrochemicals.
Used in Asymmetric Hydrogenation Reactions:
(S)-1-[(1R)-2-(DIPHENYLPHOSPHINO)FERROCENYL]ETHYLDI-TERT-BUTYLPHOSPHINE is used as a catalyst in asymmetric hydrogenation reactions, enabling the selective reduction of prochiral substrates to form chiral products with high enantioselectivity.
Used in Pharmaceutical Industry:
(S)-1-[(1R)-2-(DIPHENYLPHOSPHINO)FERROCENYL]ETHYLDI-TERT-BUTYLPHOSPHINE plays a role in the synthesis of enantiomerically pure drugs, as its catalytic properties can be harnessed to produce the desired chiral molecules with precision, which is vital for the efficacy and safety of pharmaceutical products.
Used in Agrochemical Industry:
Similarly, in the agrochemical sector, (S)-1-[(1R)-2-(DIPHENYLPHOSPHINO)FERROCENYL]ETHYLDI-TERT-BUTYLPHOSPHINE aids in the production of enantiomerically pure active ingredients for pesticides and herbicides, ensuring targeted effects on pests and weeds while minimizing environmental impact.