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5,5-dimethylcyclohexane-1,2-dione is an organic compound with the molecular formula C8H12O2. It is a white crystalline solid that is soluble in organic solvents. 5,5-dimethylcyclohexane-1,2-dione is a derivative of cyclohexane, featuring two carbonyl groups (C=O) at positions 1 and 2, and two methyl groups (CH3) attached to the carbon atoms at position 5. It is commonly used as a chemical intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other organic compounds. Due to its reactive carbonyl groups, it can participate in various chemical reactions, such as nucleophilic addition, aldol condensation, and Michael addition. The compound is also known for its potential applications in the preparation of chiral auxiliaries and ligands in asymmetric synthesis.

563-20-2

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563-20-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 563-20-2 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,6 and 3 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 563-20:
(5*5)+(4*6)+(3*3)+(2*2)+(1*0)=62
62 % 10 = 2
So 563-20-2 is a valid CAS Registry Number.

563-20-2Relevant academic research and scientific papers

COMPOUNDS FOR THE REDUCTION OF THE DELETERIOUS ACTIVITY OF EXTENDED NUCLEOTIDE REPEAT CONTAINING GENES

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, (2020/07/14)

Aspects of the present disclosure include methods of reducing the deleterious impact of a target gene in a cell, such as the deleterious activity of a mutant extended nucleotide repeat (NR) containing target gene in a cell by contacting the cell with an effective amount of a tetrahydrocarbazole compound. The deleterious activity (e.g., toxicity and/or dis-functionality of products encoded thereby) of a mutant extended NR containing target gene may be reduced, e.g., by reducing (and in some instances differentially, including selectively, reducing) the production or activity of toxic expression products (e.g., RNA or protein) encoded by the target gene. Kits and compositions for practicing the subject methods are also provided.

Oxo Complexes of Ruthenium(VI) and (VII) as Organic Oxidants

Green, Graham,Griffith, William P.,Hollinshead, David M.,Ley, Steven V.,Schroeder, Martin

, p. 681 - 686 (2007/10/02)

Oxidation of a variety of saturated and unsaturated primary and secondary alcohols by tetraoxoruthenate(VI), 2-, tetraoxoruthenate(VII), -, barium trans-trioxodihydroxoruthenium(VI), trans-Ba, dioxotrichlororuthenate(VI), -, and dioxodichlorobipyridylruthenate(VI),, has been studied; 2- may be used catalytically in conjunction with 2- under basic aqueous conditions.For some of these systems, the oxidation of several aldehydes and amines were also examined.Both 2- and - oxidise primary alcohols to carboxylic acids and secondary alcohols to ketones; the reactivity of these reagents towards unsaturated alcohols was studied in particular.The new species and also cleanly oxidise a wide range of alcohols to aldehydes and ketones without attack of double bonds.Ba functions as a heterogeneous oxidant in dichloromethane, oxidising only the most reactive alcohols to aldehydes.

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