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Methyl 2-cyclohexylidenepropanoate is a chemical compound with the molecular formula C11H18O2. It is an ester derivative of propanoic acid, characterized by its fruity and sweet aroma.

75011-86-8

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75011-86-8 Usage

Uses

Used in Food Industry:
Methyl 2-cyclohexylidenepropanoate is used as a flavoring agent for adding a pleasant scent to various food products.
Used in Perfumery:
Methyl 2-cyclohexylidenepropanoate is used as a fragrance ingredient in the production of perfumes and other scented products, due to its attractive odor profile.
Used in Pharmaceutical Industry:
Methyl 2-cyclohexylidenepropanoate is utilized in the synthesis of pharmaceuticals and other organic compounds, contributing to the development of new medications and therapeutic agents.

Check Digit Verification of cas no

The CAS Registry Mumber 75011-86-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,5,0,1 and 1 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 75011-86:
(7*7)+(6*5)+(5*0)+(4*1)+(3*1)+(2*8)+(1*6)=108
108 % 10 = 8
So 75011-86-8 is a valid CAS Registry Number.

75011-86-8Downstream Products

75011-86-8Relevant academic research and scientific papers

Carbonyl olefination with α-stannyl ester enolates: a new synthesis of α,β-unsaturated esters

Zapata, Antonio,Nunez, Beatriz M.,Ferrer, Fernando J.

, p. C9 - C11 (2007/10/02)

The reaction of α-stannyl ester enolates with carbonyl compounds is described. α,β-Unsaturated esters are obtained in good yields.A reaction mechanism is proposed.

ETUDE DE LA REACTION CHLOROCARBENE-ACETALS DE CETENES. I. SYNTHESE D'ESTERS α,β-ETHYLENIQUES.

Slougui, N.,Rousseau, G.

, p. 2643 - 2652 (2007/10/02)

The reaction of chloro, chloromethyl and chlorophenyl carbenoids with ketene alkylsilylacetals has been studied.Excellent yields of cyclopropanation were observed and the unstable chlorocyclopropanone acetals formed were thermally rearranged in high yield into α-substituted α,β-ethylenic esters.This new method for the synthesis of unsaturated esters appeared complementary of the known-ones.

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