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71423-54-6

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71423-54-6 Structure

71423-54-6 Structure
IdentificationBack Directory
[Name]

(S,S)-1,2-ETHANEDIYL-BIS-[(2-METHOXYPHENYL)-PHENYLPHOSPHINE]]-(1,5-CYCLOOCTADIENE)-RHODIUM(I)]-TETRAFLUOROBORATE
[CAS]

71423-54-6
[Synonyms]

(S,S)-(+)-1,2-Bis[(2-methoxyphenyl)phenylphosphino]ethane(1,5-cyclooctadiene)rhodium(I) terafluoroborate
(1S,2S)-()-Bis[(2-methoxyphenyl)phenylphosphino]ethane -(1,5-cyclooctadiene) rhodium(I) tetrafluorobarate
(S,S)-(+)-1,2-Bis[(o-Methoxyphenyl)(phenyl)phosphino]ethane(1,5-cyclooctadiene)rhodiuM(I) tetrafluoroborate
(S,S)-(+)-1,2-Bis[(o-Methoxyphenyl)(phenyl)phosphino]ethane(1,5-cyclooctadiene)rhodiuM(I) tetrafluoroborate,95%
(S,S)-1,2-ETHANEDIYL-BIS-[(2-METHOXYPHENYL)-PHENYLPHOSPHINE]]-(1,5-CYCLOOCTADIENE)-RHODIUM(I)]-TETRAFLUOROBORATE
[(S,S)-1,2-Ethanediyl-bis-[(2-methoxyphenyl)-phenylphosphine]]-(1,5-cyclooctadiene)-rhodium(Ⅰ)]-tetrafluoroborate
(S,S)-(+)-1,2-Bis[(o-Methoxyphenyl)(phenyl)phosphino]ethane(1,5-cyclooctadiene)rhodiuM(I)tetrafluoroborate,Min.95%
(S,S)-(+)-1,2-Bis[(o-methoxyphenyl)(phenyl)phosphino]ethane(1,5-cyclooctadiene)
rhodium(I) tetrafluoroborate, min. 95%
[Molecular Formula]

C28H28O2P2.C8H12.BF4.Rh
[MDL Number]

MFCD12198304
[MOL File]

71423-54-6.mol
[Molecular Weight]

756.371
Chemical PropertiesBack Directory
[form ]

Powder
[color ]

orange
[Sensitive ]

air sensitive
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)Corrosion (GHS05)
GHS07,GHS05
[Signal word ]

Danger
[Hazard statements ]

H302-H413-H312-H332-H318-H314
[Precautionary statements ]

P264-P270-P301+P312-P330-P501-P280-P302+P352-P312-P322-P363-P501-P261-P271-P304+P340-P312-P280-P305+P351+P338-P310-P260-P264-P280-P301+P330+P331-P303+P361+P353-P363-P304+P340-P310-P321-P305+P351+P338-P405-P501
[Safety Statements ]

22-24/25
[HS Code ]

28439000
Questions And AnswerBack Directory
[Reaction]

  1. Highly reactive enantioselective catalyst for the asymmetric hydrogenation of various substituted dehydroalanines to Nprotected aminoacids. Also, catalyst is very effective in the asymmetric reduction of pentapetides that contain unsaturated Phe or Tyr linkages to enkephalin, a brain peptide hormone.
  2. Efficient catalyst for the asymmetric reduction of enol acetates to esters.
  3. Catalyst used to prepare chiral 2-substituted succinic acid derivatives.
Reactions of 71423-54-6
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