106795-73-7 Usage
Uses
Used in Pharmaceutical Synthesis:
1-(2-chlorophenyl)cyclohexane-1-carbonitrile is used as an intermediate in the synthesis of pharmaceuticals for [application reason]. Its unique structure allows for the creation of various medicinal compounds that can target specific biological pathways.
Used in Agrochemical Synthesis:
In the agrochemical industry, 1-(2-chlorophenyl)cyclohexane-1-carbonitrile is used as a building block for the development of new agrochemicals for [application reason]. Its properties make it suitable for the production of compounds that can be used in the agricultural sector to improve crop yield and protect plants from pests.
Used in Scientific Research and Academic Studies:
1-(2-chlorophenyl)cyclohexane-1-carbonitrile is also utilized in scientific research and academic studies as a model compound for [application reason]. Its structure and properties make it an interesting subject for exploring various chemical reactions and understanding the behavior of organic nitriles and cyclohexane derivatives.
Used in Industrial Applications:
Beyond its use in pharmaceuticals and agrochemicals, 1-(2-chlorophenyl)cyclohexane-1-carbonitrile may have potential applications in other industries for [application reason]. Its versatility and unique properties could be harnessed for a range of industrial processes and products.
Check Digit Verification of cas no
The CAS Registry Mumber 106795-73-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,6,7,9 and 5 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 106795-73:
(8*1)+(7*0)+(6*6)+(5*7)+(4*9)+(3*5)+(2*7)+(1*3)=147
147 % 10 = 7
So 106795-73-7 is a valid CAS Registry Number.
106795-73-7Relevant academic research and scientific papers
Fe-catalyzed regiodivergent [1,2]-shift of α-aryl aldehydes
Gutierrez-Bonet, Alvaro,Flores-Gaspar, Areli,Martin, Ruben
supporting information, p. 12576 - 12579 (2013/09/23)
An Fe-catalyzed conversion of aldehydes to ketones via [1,2]-shift has been developed. This skeletal rearrangement shows a wide substrate scope and chemoselectivity profile while exhibiting an excellent [1,2]-aryl or [1,2]-alkyl shift selectivity that is easily switched by electronic effects.
Two New Oxindole Syntheses
Fleming, Ian,Loreto, Maria Antonietta,Wallace, Ian H.M.,Michael, Joseph P.
, p. 349 - 360 (2007/10/02)
Two oxindole syntheses are described, both starting from ketones, in which the carbonyl carbon becomes C-3 of the oxindole.The first route uses o-lithioformanilide followed by attack with cyanide ion and hydrolysis.The second uses a pinacol-type rearragement (or the γ-silyl alcohol variation) to create the quaternary centre, and involves an intramolecular displacement of fluoride ion from an unactivated benzene ring by an amide nitrogen to complete the lactam ring.The two routes are stereochemically complementary, giving different spiro-oxindoles from norbornanone.
