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1-Propanone, 1,2-diphenyl-3-(3-pyridinyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

654678-28-1

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654678-28-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 654678-28-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,5,4,6,7 and 8 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 654678-28:
(8*6)+(7*5)+(6*4)+(5*6)+(4*7)+(3*8)+(2*2)+(1*8)=201
201 % 10 = 1
So 654678-28-1 is a valid CAS Registry Number.

654678-28-1Downstream Products

654678-28-1Relevant articles and documents

NNN pincer Ru(II)-complex-catalyzed α-alkylation of ketones with alcohols

Cao, Xiao-Niu,Wan, Xiao-Min,Yang, Fa-Liu,Li, Ke,Hao, Xin-Qi,Shao, Tian,Zhu, Xinju,Song, Mao-Ping

, p. 3657 - 3668 (2018)

A series of novel ruthenium(II) complexes supported by a symmetrical NNN ligand were prepared and fully characterized. These complexes exhibited good performance in transfer hydrogenation to form new C-C bonds using alcohols as the alkylating agents, generating water as the only byproduct. A broad range of substrates, including (hetero)aryl- or alkyl-ketones and alcohols, were well tolerated under the optimized conditions. Notably, α-substituted methylene ketones were also investigated, which afforded α-branched steric hindrance products. A potential application of α-alkylation of methylene acetone to synthesize donepezil was demonstrated, which provided the desired product in 83% yield. Finally, this catalytic system could be applied to a one-pot double alkylation procedure with sequential addition of two different alcohols. The current protocol is featured with several characteristics, including a broad substrate scope, low catalyst (0.50 mol %) loadings, and environmental benignity.

CHEMICAL COMPOUNDS

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Page 108, (2010/02/06)

Compounds of formula (I):wherein variable groups are as defined within; for use in the inhibition of 11betaHSD1 are described

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