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2049086-36-2

2049086-36-2 Structure

2049086-36-2 Structure
IdentificationBack Directory
[Name]

Chloro(4-cyanophenyl){(R)-1-[(S)-2-(dicyclohexylphosphino)ferrocenyl]ethyl (diphenylphosphine)}nickel(II)
[CAS]

2049086-36-2
[Synonyms]

CHLORO(4-CYANOPHENYL){(R)-1-[(S)-2-(DICYCLOHEXYLPHOSPHINO)FERROCENYL]ETHYL(DIPHENYLPHOSPHINE)}NICKEL(II)
Chloro(4-cyanophenyl)[(R)-1-[(S)-2-(dicyclohexylphosphino)ferrocenyl]ethyldiphenylphosphine]nickel(II) >=95%
[Molecular Formula]

C43H48ClFeNNiP2
[MDL Number]

MFCD31619173
[MOL File]

2049086-36-2.mol
[Molecular Weight]

785.76
Chemical PropertiesBack Directory
[form ]

solid
[color ]

orange
[SMILES]

C[Ni+]C1=CC=C(C#N)C=C1.[C]2(CP(C3=CC=CC=C3)C4=CC=CC=C4)[C][C][C][C]2P(C5CCCCC5)C6CCCCC6.[C]7[C][C][C][C]7.[Fe]
Safety DataBack Directory
[WGK Germany ]

WGK 3
[Storage Class]

11 - Combustible Solids
Questions And AnswerBack Directory
[Uses]

Chloro(4-cyanophenyl){(R)-1-[(S)-2-(dicyclohexylphosphino)ferrocenyl]ethyl (diphenylphosphine)}nickel(II) is useful in these fields:
  1. Versatile air-stable low cost nickel catalyst alternative to palladium for carbon-carbon and carbonheteroatom cross-coupling reactions.
  2. Used to react substituted aryl and heteroaryl halides and tosylates with ammonia to produce diverse aryl and heteroaryl amines
  3. Used in monoarylation experiments using commercially available ammonia gas, ammonium salts or ammonia stock solutions
  4. Catalyzes the coupling of aryl chlorides with gaseous amines in the form of their hydrochloride salts 
Hazard InformationBack Directory
[reaction suitability]

core: nickel
reaction type: Cross Couplings
reagent type: catalyst
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