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1-(1-ethoxyvinyl)-4-tert-butylcylohex-1-ene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

125950-34-7

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125950-34-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 125950-34-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,5,9,5 and 0 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 125950-34:
(8*1)+(7*2)+(6*5)+(5*9)+(4*5)+(3*0)+(2*3)+(1*4)=127
127 % 10 = 7
So 125950-34-7 is a valid CAS Registry Number.

125950-34-7Relevant academic research and scientific papers

Regiocontrolled Cyclohexenone Annulation via Acylation of a Ketone Carbonyl

Paquette, Leo A.,Ra, Choon Sup,Edmonson, Scott D.

, p. 2443 - 2445 (2007/10/02)

1-(1-Ethoxyvinyl)cycloalkenes, readily available by palladium-catalyzed condensation of enol triflates with ethyl vinyl ether or its α-trimethylstannyl derivative, enter into Diels-ALder reaction with (Z)-1,2-bis(phenylsulfonyl)ethylene.These adducts unde

Palladium-Catalyzed Coupling Reactions of (α-Ethoxyvinyl)trimethylstannane with Vinyl and Aryl Triflates

Kwon, Hyok Boong,McKee, Blain H.,Stille, J. K.

, p. 3114 - 3118 (2007/10/02)

The palladium-catalyzed cross-coupling reaction of vinyl triflates and halides with (α-ethoxyvinyl)trimethylstannane gives high yields of 2-ethoxy 1,3-dienes, which can be hydrolyzed to the corresponding α,β-unsaturated ketones.Aryl triflates undergo an analogous coupling reaction, providing a facile method for replacing the hydroxyl group of a phenol by an acyl group.The use of (α-ethoxyvinyl)trimethylstannane in palladium-catalyzed carbonylative coupling gives rise to vinyl and aryl α-ethoxyvinyl ketones and indirectly to the corresponding α-diketones (which result from their hydrolysis) and glyoxylates (which result from their ozonolysis).

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