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3-hydroxy-3-(pyridin-4-yl)-5-methoxy-2-phenyl-2,3-dihydro-1H-isoindol-1-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

154822-32-9

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154822-32-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 154822-32-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,4,8,2 and 2 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 154822-32:
(8*1)+(7*5)+(6*4)+(5*8)+(4*2)+(3*2)+(2*3)+(1*2)=129
129 % 10 = 9
So 154822-32-9 is a valid CAS Registry Number.

154822-32-9Downstream Products

154822-32-9Relevant academic research and scientific papers

Application of organolithium and related reagents in synthesis. Part 221. Synthetic strategies based on ortho-aromatic metallation. A concise regiospecific conversion of benzoic acids into the 4-pyridyl-2h-phthalazin- 1-ones

Brzezinski,Epsztajn,Bakalarz,LAjszczak,Malinowski

, p. 457 - 473 (2007/10/03)

The synthesis of phthalazin-1-ones 6, 7, 8 via the reaction of 3- hydroxyisoindolin-1-ones 3, 4, 5 with hydrazine hydrate is described. Starting compounds 3, 4, 5 were regiospecifically prepared upon the lithiation (n-BuLi) of the benzanilides 1 and subsequently the reaction of the dilithiated anilides 2 with methyl pyridinecarboxylates.

Application of organolithium and related reagents in synthesis. Part 14. Synthetic strategies based on aromatic metallation. A concise regiospecific conversion of benzole acids into their ortho-pyridoyl derivatives

Epsztajn, Jan,Jozwiak, Andrzej,Krysiak, Jerzy A.

, p. 2907 - 2916 (2007/10/02)

The synthesis of the 3-hydroxy-3-pyridyl-isoindolin-1-ones (5) and (6) via metallation (n-BuLi) of the benzanilides (1), and then the reaction of the generated bis lithiated anilides (2) with N,N-dimethylamides or methyl esters of pyridinecarboxylic acids (benzoylation reagents), and subsequent acidic hydrolysis of (5) and (6) as a way (general synthetic strategy) of regiospecific transformation of benzoic acids into their ortho-benzoylated derivatives, is described.

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