Molecular Weight
802.88
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- Chloro(4-cyanophenyl)[(R)-1-[(S)-2-(dicyclohexylphosphino)ferrocenyl]ethyldicyclohexylphosphine]nickel(II)
Chloro(4-cyanophenyl)[(R)-1-[(S)-2-(dicyclohexylphosphino)ferrocenyl]ethyldicyclohexylphosphine]nickel(II)
Catalog Number
ACM2049086351
Product Name
Chloro(4-cyanophenyl)[(R)-1-[(S)-2-(dicyclohexylphosphino)ferrocenyl]ethyldicyclohexylphosphine]nickel(II)
CAS
2049086-35-1
Application
Chloro(4-cyanophenyl)[(R)-1-[(S)-2-(dicyclohexylphosphino)ferrocenyl]ethyldicyclohexylphosphine]nickel(II) serves as a versatile and air-stable catalyst, positioned as a cost-effective alternative to palladium for driving carbon-carbon and carbon-heteroatom cross-coupling reactions. Its primary function is to enable the amination of aryl and heteroaryl halides, tosylates, bromides, sulfonates, and carbamates with ammonia, thereby facilitating the production of a diverse range of aryl and heteroaryl amines. This catalyst is also effective in monoarylation processes employing commercially available ammonia gas, ammonium salts, or ammonia stock solutions. The catalyst's ability to couple aryl chlorides with gaseous amines, presented as their hydrochloride salts, underscores its utility and flexibility in various synthetic applications.
April 16, 2025
Excellent Nickel Catalyst for Efficient Cross-Coupling Reactions
I've used Alfa Chemistry's nickel catalyst for monoarylation experiments, reacting aryl halides with ammonia. It's a cost-effective, air-stable alternative to palladium for producing diverse amines in research. Highly recommend for its versatility.
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