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(+)-cis-(3S,4S)-3,4-dihydroxy-3,4-dihydro-2-quinolone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

206563-13-5

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206563-13-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 206563-13-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,6,5,6 and 3 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 206563-13:
(8*2)+(7*0)+(6*6)+(5*5)+(4*6)+(3*3)+(2*1)+(1*3)=115
115 % 10 = 5
So 206563-13-5 is a valid CAS Registry Number.

206563-13-5Upstream product

206563-13-5Downstream Products

206563-13-5Relevant academic research and scientific papers

Dioxygenase-catalyzed cis-dihydroxylation of pyridine-ring systems

Boyd, Derek R.,Sharma, Narain D.,Modyanova, Ludmila V.,Carroll, Jonathan G.,Malone, John F.,Allen, Christopher C.R.,Hamilton, John T.G.,Gibson, David T.,Parales, Rebecca E.,Dalton, Howard

, p. 589 - 600 (2007/10/03)

Toluene dioxygenase-catalyzed dihydroxylation, in the carbocyclic rings of quinoline, 2-chloroquinoline, 2-methoxyquinoline, and 3-bromoquinoline, was found to yield the corresponding enantiopure cis-5,6- and -7,8-dihydrodiol metabolites using whole cells

Dioxygenase-catalysed cis-dihydrodiol formation in the carbo- and hetero-cyclic rings of quinolines

Boyd,Sharma,Carroll,Malone,Mackerracher,Allen

, p. 683 - 684 (2007/10/03)

Evidence of enzyme-catalysed cis-dihydroxylation in the pyridine (3,4-bond) and benzene rings (5,6- and 7,8-bonds) of quinoline and 2-substituted quinolines is examined in light of the isolation of a heterocyclic cis-diol derivative of 2-quinolone, as a single enantiomer of opposite absolute configuration to that found for the enantiopure carbocyclic cis-diol metabolites from quinolines.

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