(R)-1-(DIPHENYLPHOSPHINO)-2-[(S)-4-ISOPROPYL-2-OXAZOLIN-2-YL]FERROCENE TRIPHENYLPHOSPHINE RUTHENIUM(II) CHLORIDE COMPLEX

(R)-1-(DIPHENYLPHOSPHINO)-2-[(S)-4-ISOPROPYL-2-OXAZOLIN-2-YL]FERROCENE TRIPHENYLPHOSPHINE RUTHENIUM(II) CHLORIDE COMPLEX Basic information
Reaction
Product Name:(R)-1-(DIPHENYLPHOSPHINO)-2-[(S)-4-ISOPROPYL-2-OXAZOLIN-2-YL]FERROCENE TRIPHENYLPHOSPHINE RUTHENIUM(II) CHLORIDE COMPLEX
Synonyms:(S)-2-[(SP)-2-(Diphenylphosphino)ferrocenyl]-4-isopropyl-2-oxazoline triphenylphosphine ruthenium(II) dichloride Complex >=97%;(S)-2-[(SP)-2-(Diphenylphosphino)ferrocenyl]-4-isopropyl-2-oxazolinetriphenylphosphine rutheni;(-)-DICHLORO[(4S)-4-(I-PROPYL)-2-[(S)-2-(DIPHENYLPHOSPHINO)FERROCENYL]OXAZOLINE](TRIPHENYLPHOSPHINE)RUTHENIUM (II);(S)-2-[(S)-2-(DIPHENYLPHOSPHINO)FERROCENYL]-4-ISOPROPYL-2-OXAZOLINE TRIPHENYLPHOSPHINE RUTHENIUM(II) DICHLORIDE COMPLEX;(R)-1-(DIPHENYLPHOSPHINO)-2-[(S)-4-ISOPROPYL-2-OXAZOLIN-2-YL]FERROCENE TRIPHENYLPHOSPHINE RUTHENIUM(II) CHLORIDE COMPLEX;NAUD CATALYST SK-N003-2Z;(-)-Dichloro[(4S)-4-(i-propyl)-2-{(S)-2-(diphenylphosphino)ferrocenyl}oxazoline]
(triphenylphosphine)ruthenium (II)
;(S)-2-[(S)-2-(Diphenylphosphino)ferrocenyl]-4-isopropyl-2-oxazoline triphenylpho
CAS:212133-11-4
MF:C46H43Cl2FeNOP2Ru10*
MW:915.61
EINECS:
Product Categories:Ru;metal phosphine complex
Mol File:212133-11-4.mol
(R)-1-(DIPHENYLPHOSPHINO)-2-[(S)-4-ISOPROPYL-2-OXAZOLIN-2-YL]FERROCENE TRIPHENYLPHOSPHINE RUTHENIUM(II) CHLORIDE COMPLEX Structure
(R)-1-(DIPHENYLPHOSPHINO)-2-[(S)-4-ISOPROPYL-2-OXAZOLIN-2-YL]FERROCENE TRIPHENYLPHOSPHINE RUTHENIUM(II) CHLORIDE COMPLEX Chemical Properties
alpha -1127° (c 0.1, CHCl3)
storage temp. under inert gas (nitrogen or Argon) at 2-8°C
form Powder
color orange-brown
Safety Information
WGK Germany 3
HS Code 28439000
MSDS Information
(R)-1-(DIPHENYLPHOSPHINO)-2-[(S)-4-ISOPROPYL-2-OXAZOLIN-2-YL]FERROCENE TRIPHENYLPHOSPHINE RUTHENIUM(II) CHLORIDE COMPLEX Usage And Synthesis
Reaction
  1. Catalyst used for the oxidative kinetic resolution of racemic alcohols.
  2. Catalyst used for the extremely high enantioselective transfer hydrogenation of ketones and the oxidative kinetic resolution of alcohols.
  3. Catalyst used for the asymmetric hydrosilylation of ketones and imine.
Chemical PropertiesOrange powder
General Descriptionsold in collaboration with Solvias AG
(R)-1-(DIPHENYLPHOSPHINO)-2-[(S)-4-ISOPROPYL-2-OXAZOLIN-2-YL]FERROCENE TRIPHENYLPHOSPHINE RUTHENIUM(II) CHLORIDE COMPLEX Preparation Products And Raw materials
METHYL 2-METHYLPROPANIMIDIC ACID HYDROCHLORIDE ETHYL BUTYRIMIDATE HYDROCHLORIDE CYCLOPENTANECARBOXIMIDIC ACID ETHYL ESTER 4,5-dihydro-2-propyloxazole Ferrocenemethanol Ruthenium ETHYL PENTANIMIDATE BIS(CYCLOPENTADIENYL)RUTHENIUM 2-ISOPROPYL-2-OXAZOLINE Oxazoline (R)-1-(DIPHENYLPHOSPHINO)-2-[(S)-4-ISOPROPYL-2-OXAZOLIN-2-YL]FERROCENE TRIPHENYLPHOSPHINE RUTHENIUM(II) CHLORIDE COMPLEX

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