Welcome to LookChem.com Sign In|Join Free
  • or
(S)-1-[(R)-2-(Dicyclohexylphosphino)-Ferrocenyl]EthylDicyclohexylPhosphine is an organometallic compound characterized by its unique chiral configuration and the presence of a ferrocene moiety. (S)-1-[(R)-2-(DICYCLOHEXYLPHOSPHINO)-FERROCENYL]ETHYLDICYCLOHEXYLPHOSPHINE is distinguished by an (R) configuration at the ferrocene center and an (S) configuration at the ethyl group. Its structure includes two dicyclohexylphosphine groups that act as coordinating sites for transition metals, while the ferrocene moiety contributes stability and electron-donating properties. These features render the compound a versatile ligand in the realm of transition metal catalysis and asymmetric synthesis.

246231-77-6

Post Buying Request

246231-77-6 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

246231-77-6 Usage

Uses

Used in Pharmaceutical Industry:
(S)-1-[(R)-2-(Dicyclohexylphosphino)-Ferrocenyl]EthylDicyclohexylPhosphine is utilized as a chiral ligand for the synthesis of chiral molecules and pharmaceuticals. Its unique configuration allows for selective interactions with certain substrates and transition metals, which is crucial in the production of enantiomerically pure compounds. This selectivity is particularly valuable in the development of single-enantiomer drugs, as it can lead to more effective and safer medications with fewer side effects.
Used in Chemical Catalysis:
In the field of chemical catalysis, (S)-1-[(R)-2-(Dicyclohexylphosphino)-Ferrocenyl]EthylDicyclohexylPhosphine serves as a ligand in transition metal catalysis. Its ability to coordinate with transition metals and facilitate selective reactions makes it an important component in various catalytic processes. This can lead to more efficient and cleaner chemical syntheses, reducing waste and improving the overall sustainability of chemical production.
Used in Asymmetric Synthesis:
(S)-1-[(R)-2-(Dicyclohexylphosphino)-Ferrocenyl]EthylDicyclohexylPhosphine is also employed in asymmetric synthesis, where it plays a critical role in the production of enantiomerically enriched compounds. Its chiral nature enables the creation of molecules with specific three-dimensional arrangements, which is essential for the biological activity of many pharmaceuticals and agrochemicals. This application is particularly relevant in the development of new drugs and the improvement of existing ones, as it can lead to more targeted and effective treatments.

Check Digit Verification of cas no

The CAS Registry Mumber 246231-77-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,4,6,2,3 and 1 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 246231-77:
(8*2)+(7*4)+(6*6)+(5*2)+(4*3)+(3*1)+(2*7)+(1*7)=126
126 % 10 = 6
So 246231-77-6 is a valid CAS Registry Number.
InChI:InChI=1/C31H51P2.C5H5.Fe/c1-25(32(26-15-6-2-7-16-26)27-17-8-3-9-18-27)30-23-14-24-31(30)33(28-19-10-4-11-20-28)29-21-12-5-13-22-29;1-2-4-5-3-1;/h14,23-29H,2-13,15-22H2,1H3;1-5H;/t25-;;/m0../s1

246231-77-6SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name cyclopenta-1,3-diene,dicyclohexyl-[(1S)-1-(2-dicyclohexylphosphanylcyclopenta-2,4-dien-1-yl)ethyl]phosphane,iron(2+)

1.2 Other means of identification

Product number -
Other names (S)-1-[(RP)-2-(Dicyclohexylphosphino)ferrocenyl]ethyldicyclohexylphosphine

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:246231-77-6 SDS

246231-77-6Downstream Products

246231-77-6Relevant academic research and scientific papers

Rhodium-Catalyzed Asymmetric Allylation of Malononitriles as Masked Acyl Cyanide with Allenes: Efficient Access to β,γ-Unsaturated Carbonyls

Grugel, Christian P.,Breit, Bernhard

supporting information, p. 15223 - 15226 (2018/09/25)

A rhodium-catalyzed regio- and enantioselective intermolecular allylation of malononitriles as masked acyl cyanides (MAC) with terminal and symmetrical internal allenes is reported. A RhI/Josiphos catalytic system combined with subsequent oxidative degradation of the primary adducts enables a straightforward access to α-branched, β,γ-unsaturated carbonyl compounds. The present protocol exhibits perfect atom economy in the allylation step and is characterized by a great functional group compatibility. Furthermore, the use of α-substituted malononitriles allowed for the construction of all-carbon quaternary centers.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 246231-77-6