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trans-Bis(dicyclohexylphenylphosphino)nickel(II) chloride, 99% is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

19232-03-2

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19232-03-2 Usage

Reactions

Catalyst used for the coupling of alkenes, aldehydes, and silyl triflates. Catalyst used for the cross-coupling of aryl Grignard reagents with aromatic ethers.

Check Digit Verification of cas no

The CAS Registry Mumber 19232-03-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,2,3 and 2 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 19232-03:
(7*1)+(6*9)+(5*2)+(4*3)+(3*2)+(2*0)+(1*3)=92
92 % 10 = 2
So 19232-03-2 is a valid CAS Registry Number.

19232-03-2Relevant academic research and scientific papers

NICKEL PRE-CATALYSTS AND RELATED COMPOSITIONS AND METHODS

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Page/Page column 24; 41, (2015/05/26)

Described herein are nickel pre-catalysts and related compositions and methods. The nickel pre-catalysts may be activated to form catalysts which may be utilized in organic reactions.

Simplifying nickel(0) catalysis: An air-stable nickel precatalyst for the internally selective benzylation of terminal alkenes

Standley, Eric A.,Jamison, Timothy F.

supporting information, p. 1585 - 1592 (2013/03/14)

The synthesis and characterization of the air-stable nickel(II) complex trans-(PCy2Ph)2Ni(o-tolyl)Cl is described in conjunction with an investigation of its use for the Mizoroki-Heck-type, room temperature, internally selective coupling of substituted benzyl chlorides with terminal alkenes. This reaction, which employs a terminal alkene as an alkenylmetal equivalent, provides rapid, convergent access to substituted allylbenzene derivatives in high yield and with regioselectivity greater than 95:5 in nearly all cases. The reaction is operationally simple, can be carried out on the benchtop with no purification or degassing of solvents or reagents, and requires no exclusion of air or water during setup. Synthesis of the precatalyst is accomplished through a straightforward procedure that employs inexpensive, commercially available reagents, requires no purification steps, and proceeds in high yield.

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