Dichlorobis(dicyclohexylphenylphosphine)nickel(II)

95%

Reagent Code: #174441
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CAS Number 19232-03-2

science Other reagents with same CAS 19232-03-2

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Weight 678.37 g/mol
Formula C₃₆H₅₄Cl₂NiP₂
badge Registry Numbers
MDL Number MFCD25563227
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as a catalyst in cross-coupling reactions, particularly in the formation of carbon-carbon bonds. It is effective in reactions such as Kumada and Negishi couplings, where it facilitates the coupling of organozinc or organomagnesium compounds with aryl or vinyl halides. Its stability and selectivity make it suitable for use in the synthesis of complex organic molecules, including pharmaceuticals and fine chemicals. The ligand structure enhances catalytic activity by stabilizing the nickel center and promoting oxidative addition. Commonly employed in inert atmosphere reactions due to sensitivity to air and moisture.

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inventory 50mg
10-20 days ฿2,410.00

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Dichlorobis(dicyclohexylphenylphosphine)nickel(II)
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Used as a catalyst in cross-coupling reactions, particularly in the formation of carbon-carbon bonds. It is effective in reactions such as Kumada and Negishi couplings, where it facilitates the coupling of organozinc or organomagnesium compounds with aryl or vinyl halides. Its stability and selectivity make it suitable for use in the synthesis of complex organic molecules, including pharmaceuticals and fine chemicals. The ligand structure enhances catalytic activity by stabilizing the nickel center and p

Used as a catalyst in cross-coupling reactions, particularly in the formation of carbon-carbon bonds. It is effective in reactions such as Kumada and Negishi couplings, where it facilitates the coupling of organozinc or organomagnesium compounds with aryl or vinyl halides. Its stability and selectivity make it suitable for use in the synthesis of complex organic molecules, including pharmaceuticals and fine chemicals. The ligand structure enhances catalytic activity by stabilizing the nickel center and promoting oxidative addition. Commonly employed in inert atmosphere reactions due to sensitivity to air and moisture.

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