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360048-63-1

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360048-63-1 Structure

360048-63-1 Structure
IdentificationBack Directory
[Name]

(R)-(-)-1-[(S)-2-(DI(3,5-DIMETHYL-4-METHOXYPHENYL)PHOSPHINO)FERROCENYL]ETHYLDICYCLOHEXYLPHOSPHINE
[CAS]

360048-63-1
[Synonyms]

(R)-1-{(S)-2-[Bis(4-Methoxy-3,5-diMeth
(R)-1-{(S)-2-[Bis(4-methoxy-3,5-dimethylphenyl)phosphino]ferrocenyl}ethyldicyclo
(R)-1-{(SP)-2-[Bis(4-Methoxy-3,5-diMethylphenyl)phosphino]ferrocenyl}ethyldicyclohexylphosphine
(R)-1-[(S)-2-Di-(4-methoxy-3,5-dimethylphenyl-phosphino)ferrocenyl]-ethyl-dicyclohexylphosphine
(R)-(-)-1-[(S)-2-(DI(3,5-DIMETHYL-4-METHOXYPHENYL)PHOSPHINO)FERROCENYL]ETHYLDICYCLOHEXYLPHOSPHINE
(R)-(-)-1-{(S)-2-[Bis(3,5-diMethyl-4-Methoxyphenyl)phosphino]ferrocenyl}ethyldicyclohexylphosphine
(R)-(-)-1-{(SP)-2-[Bis(3,5-dimethyl-4-methoxyphenyl)phosphino]ferrocenyl}ethyldicyclohexylphosphine
(1R)-1-[Bis(4-methoxy-3,5-dimethylphenyl)phosphino]-2-[(1R)-1-(dicyclohexylphosphino)ethyl]ferrocene
(R)-1-{(SP)-2-[Bis(4-methoxy-3,5-dimethylphenyl)phosphino]ferrocenyl}ethyldicyclohexylphosphine >=97%
(R)-(-)-1-{(S)-2-[Bis(3,5-dimethyl-4-methoxyphenyl)phosphino]ferrocenyl}ethyldicyclohexylphosphine,min.97%
(R)-(-)-1-{(S)-2-[Bis(3,5-dimethyl-4-methoxyphenyl)phosphino]ferrocenyl}ethyldicyclohexylphosphine, min. 97%
(r,r)-1-[1-(dicyclohexylphosphino)ethyl]-2-[bis(4-methoxy-3,5-dimethylphenyl)phosphino]ferrocene (acc to cas)
(R)-(-)-1-{(S)-2-[Bis(3,5-dimethyl-4-methoxyphenyl)phosphino]ferrocenyl}
ethyldicyclohexylphosphine, min. 97%
[Molecular Formula]

C42H56FeO2P2 10*
[MDL Number]

MFCD03426995
[MOL File]

360048-63-1.mol
[Molecular Weight]

710.69
Chemical PropertiesBack Directory
[alpha ]

-270° ±10° (c 0.5, CHCl3)
[form ]

Powder
[color ]

orange
Hazard InformationBack Directory
[Chemical Properties]

Orange powder
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P261-P280-P301+P312-P302+P352-P305+P351+P338
[WGK Germany ]

3
[HS Code ]

29319090
Questions And AnswerBack Directory
[Uses]

  2. Homogeneous chiral nickel-catalyzed asymmetric hydrogenation of substituted aromatic α-aminoketone hydrochlorides through dynamic kinetic resolution.
  4. Pd/Josiphos-catalyzed enantioselective α-arylation of silyl ketene acetals.
  6. Ligand used in the cobalt-catalyzed asymmetric addition of silylacetylenes to 1,1-disubstitued allenes.
addition of silylacetylenes to 1,1-disubstitued allenes
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