(R)-(+)-[(R)-2-Dicyclohexylphosphinoferrocenyl](N,N-dimethylamino)(2-dicyclohexylphosphinophenyl)met

Introduction：Basic information about (R)-(+)-[(R)-2-Dicyclohexylphosphinoferrocenyl](N,N-dimethylamino)(2-dicyclohexylphosphinophenyl)met, including its chemical name, molecular formula, synonyms, physicochemical properties, and safety information, etc.

(R)-(+)-[(R)-2-Dicyclohexylphosphinoferrocenyl](N,N-dimethylamino)(2-dicyclohexylphosphinophenyl)methane, min. 97% Basic information

• Product Name: (R)-(+)-[(R)-2-Dicyclohexylphosphinoferrocenyl](N,N-dimethylamino)(2-dicyclohexylphosphinophenyl)methane, min. 97%
• Synonyms: (R)-(+)-[(R)-2-DicycL;(R)-1-Dicyclohexylphosphino-2-[(R)-(N,N-dimethylamino)[2-(dicyclohexylphosphino)phenyl]methyl]ferrocene;SL-T002-1;(1S)-1-(Dicyclohexylphosphino)-2-[(R)-[2-(dicyclohexylphosphino)phenyl](dimethylamino)methyl]ferrocene;(1Rp)-1-(Dicyclohexylphosphino)-2-[(R)-[2-(dicyclohexylphosphino)phenyl](dimethylamino)methyl]ferrocene;1-(Dicyclohexylphosphino)-2-[(R)-[2-(dicyclohexylphosphino)phenyl](dimethylamino)methyl] ferrocene;(R_P)-1-Dicyclohexylphosphino-2-[(R)-α-(dimethylamino)-2-(dicyclohexylphosphino)benzyl]ferrocene;(R)-(+)-[(R)-2-Dicyclohexylphosphinoferrocenyl](N,N-dimethylamino)(2-dicyclohexylphosphinophenyl)methane, min. 97%
• CAS: 1156547-61-3
• MF: C43H57FeNP2
• MW: 705.73
• Mol File: 1156547-61-3.mol

(R)-(+)-[(R)-2-Dicyclohexylphosphinoferrocenyl](N,N-dimethylamino)(2-dicyclohexylphosphinophenyl)methane, min. 97% Chemical Properties

• alpha: +110° ±10° (c 0.5, CHCl3)
• storage temp.: under inert gas (nitrogen or Argon) at 2-8°C
• form: Powder
• color: orange
• Stability: store cold
• InChIKey: DOWXTPVXDDGHHG-VROLVAQFSA-N
• CAS DataBase Reference: 1156547-61-3

Safety Information

• WGK Germany: WGK 3
• Storage Class: 11 - Combustible Solids

(R)-(+)-[(R)-2-Dicyclohexylphosphinoferrocenyl](N,N-dimethylamino)(2-dicyclohexylphosphinophenyl)methane, min. 97% Usage And Synthesis

Reaction

1. Ligand for Rh and Ru-catalzyed hydrogenation of alkenes and ketones.
2. Rh-catalyzed intermolecular [4+2].
3. Enantioselective reductive coupling of 1,3-enynes to heterocyclic aromatic aldehydes and ketones.