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Methanone, 1-cycloocten-1-ylphenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

67788-08-3

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67788-08-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 67788-08-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,7,7,8 and 8 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 67788-08:
(7*6)+(6*7)+(5*7)+(4*8)+(3*8)+(2*0)+(1*8)=183
183 % 10 = 3
So 67788-08-3 is a valid CAS Registry Number.

67788-08-3Relevant academic research and scientific papers

Enones from Acid Fluorides and Vinyl Triflates by Reductive Nickel Catalysis

Pan, Feng-Feng,Guo, Peng,Li, Chun-Ling,Su, Peifeng,Shu, Xing-Zhong

supporting information, p. 3701 - 3705 (2019/05/24)

A nickel-catalyzed reductive coupling between acid fluorides and vinyl triflates has been described. This method provides an efficient access to various enones and avoids the requirement for acyl or vinyl metallic reagents in the conventional approaches.

1,2-Addition of α,α,α-trichlorotoluene to ketones via a Mg Barbier reaction in DMF: New route to cycloalk-1-en-1-yl and alk-1-en-1-yl phenyl ketones

Aaziz, Akima,Oudeyer, Sylvain,Leonel, Eric,Paugam, Jean Paul,Nedelec, Jean-Yves

, p. 1147 - 1154 (2008/02/01)

The reductive cyclocondensation of α,α,α-trichlorotoluene to enolisable ketones enables the preparation of (cyclo)alken-1-en-1-yl phenyl ketones via the formation of an intermediate chlorooxirane. Copyright Taylor & Francis Group, LLC.

Regiospecific acylations of aromatics and selective reductions of azobenzenes over hydrated zirconia

Patil,Jnaneshwara,Sabde,Dongare,Sudalai,Deshpande

, p. 2137 - 2140 (2007/10/03)

Hydrated zirconia has been found to be an efficient and reusable catalyst for the regiospecific acylations of arenes and selective reductions of azobenzenes to produce benzophenones and hydrazabenzenes respectively.

Conversion of ketone trimethylsilylcyanohydrins to several types of compounds

Ohta,Yamashita,Arita,Kajiura,Kawasaki,Noda,Izumi

, p. 1294 - 1301 (2007/10/02)

Cyclic ketone O-trimethylsilylcyanohydrins (2) were prepared and converted to various compounds: α-hydroxyketones (3), dehydroxylated ketones (4), α,β-unsaturated ketones (9), tricyclic ketones (10), 1-ethoxycarbonyl-4- phenyl-1,2,4a,5,6,7,8,8a-octahydro-2-naphthalenone (13), 1- phenylperhydroisocoumarin (18) and 1,2,3,4,4a,10,11,11a-octahydro-5h- benzo[a,d]cyclohepten-10-one (20).

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