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Ethanone, 1-[2'-(diphenylphosphinyl)[1,1'-biphenyl]-4-yl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

402822-63-3

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402822-63-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 402822-63-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,0,2,8,2 and 2 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 402822-63:
(8*4)+(7*0)+(6*2)+(5*8)+(4*2)+(3*2)+(2*6)+(1*3)=113
113 % 10 = 3
So 402822-63-3 is a valid CAS Registry Number.

402822-63-3Downstream Products

402822-63-3Relevant academic research and scientific papers

Palladium-catalyzed R2(O)P directed C(sp2)-H acetoxylation

Zhang, Heng,Hu, Rong-Bin,Zhang, Xiao-Yu,Li, Shi-Xia,Yang, Shang-Dong

supporting information, p. 4686 - 4689 (2014/05/06)

A novel and efficient Pd-catalyzed C-H acetoxylation is described. The approach uses R2(O)P as a directing group to synthesize various substituted 2′-phosphorylbiphenyl-2-OAc compounds. Notably, the reaction exhibits smooth operation under mild conditions and shows good functional group tolerance. Products are obtained with high selectivity and yields. This journal is the Partner Organisations 2014.

Palladium-catalyzed direct synthesis of phosphole derivatives from triarylphosphines through cleavage of carbon-hydrogen and carbon-phosphorus bonds

Baba, Katsuaki,Tobisu, Mamoru,Chatani, Naoto

supporting information, p. 11892 - 11895 (2013/11/19)

(Phosp)hole in one: A palladium-catalyzed synthesis for directly assembling phosphole skeletons from triarylphosphines through C-H and C-P bond cleavage was developed. This approach overcomes several of the limitations of the so far reported methods. Phospholes bearing a range of functionalities (including Br, F, CO2Me, Ac, and CN) and an array of fused rings (naphthalenes, anthracenes, furans, and pyrroles) can be easily synthesized. Copyright

Palladium-catalysed synthesis of biaryl phosphines

Baillie, Colin,Xiao, Jianliang

, p. 4159 - 4168 (2007/10/03)

Monodentate, biphenyl-type phosphines have emerged as a powerful class of ligands in homogeneous catalysis. Synthetic methods for these ligands are limited, however. We report that the palladium-catalysed Suzuki coupling of OPR2(o-C6H4X) (R=Ph, t-Bu; X=Br, I) with arylboronic acids affords a variety of biaryl phosphine oxides including those that contain heterocycles. The corresponding phosphines are readily obtained by treatment with HSiCl3. The methodology provides an easy entry to monodentate biaryl and heterobiaryl Poverlapping logical AND signX (X=N, O, S) phosphines with diverse steric and electronic properties.

Synthesis of biphenyl-based phosphines by Suzuki coupling

Baillie, Colin,Chen, Weiping,Xiao, Jianliang

, p. 9085 - 9088 (2007/10/03)

A series of phosphine oxides has been synthesised by the palladium-catalysed Suzuki coupling of arylboronic acids with OPPh2(o-C6H4Br). On reduction with trichlorosilane, functionalised, biphenyl-based phosphine ligands were obtained in good yields. Our preliminary results indicate these ligands to be effective for palladium-catalysed C-C coupling reactions including the formation of their own oxides.

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