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(E)-1-Cyclohexyl-pent-3-en-1-one is an organic compound characterized by a cyclohexyl group attached to a pent-3-en-1-one moiety. This molecule features a cyclohexane ring with a double bond between the third and fourth carbon atoms of the pentene chain, and a ketone group (carbonyl) at the first position. The "E" configuration indicates that the substituents on the double bond are arranged in a trans orientation. (E)-1-Cyclohexyl-pent-3-en-1-one is known for its unique chemical properties and potential applications in various fields, such as pharmaceuticals and fragrances, due to its distinct structure and reactivity.

79237-36-8

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79237-36-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 79237-36-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,9,2,3 and 7 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 79237-36:
(7*7)+(6*9)+(5*2)+(4*3)+(3*7)+(2*3)+(1*6)=158
158 % 10 = 8
So 79237-36-8 is a valid CAS Registry Number.

79237-36-8Downstream Products

79237-36-8Relevant academic research and scientific papers

SYNTHESE STEREOSPECIFIQUE DE BUTENYL-2 CETONES ET DE L'ACIDE BUTENE-2 SULFONIQUE

Grignon-Dubois, Micheline,Dunogues, Jacques,Calas, Raymond

, p. 2883 - 2884 (2007/10/02)

1-Trimethylsilyl 2-methylcyclopropane cis or trans resulting from the silylation of 1-bromo 1-propene is a convenient regio- and stereospecific precursor of β,γ-unsaturated Z or E ketones and 2-butene sulfonic acid.

Acylation du (cyclopropylmethyl)trimethylsilane. Une nouvelle voie d'acces aux enones non conjuguees

Grignon-Dubois, M.,Dunogues, J.,Calas, R.

, p. 802 - 806 (2007/10/02)

Acylation of (cyclopropylmethyl)trimethylsilane using RCOCl/AlCl3 (R: saturated hydrocarbon group) constitutes a mild, convenient route to β,γ-unsaturated ketones free from the conjugated isomers.With α,β-unsaturated acyl chlorides a competitive reaction between the C-H and C-Si allylic cleavage is observed whereas chloroacetyl chloride affords the γ,δ-ethylenic corresponding ketone.A mechanism involving the catalytic role of HCl in the formation of β,γ-unsaturated and chloroketones is proposed.

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