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Cyclohexaneacetic acid, 2-ethylidene-, methyl ester, (Z)is a chemical compound that is widely recognized for its distinctive fruity and floral aroma. It is synthesized through the esterification of cyclohexaneacetic acid with methanol, resulting in a Z isomer, where the two substituents on the double bond are positioned on the same side of the molecule. Cyclohexaneacetic acid, 2-ethylidene-, methyl ester, (Z)is frequently utilized as a fragrance ingredient and flavoring agent in a variety of products, including perfumes, cosmetics, and food items. While it is generally considered safe for use, some individuals may experience skin irritation or sensitization.

90173-11-8

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90173-11-8 Usage

Uses

Used in Perfumery and Cosmetics Industry:
Cyclohexaneacetic acid, 2-ethylidene-, methyl ester, (Z)is used as a fragrance ingredient for its appealing fruity and floral scent, enhancing the olfactory profile of perfumes and cosmetics.
Used in Food Industry:
In the food industry, Cyclohexaneacetic acid, 2-ethylidene-, methyl ester, (Z)is used as a flavoring agent to impart a pleasant aroma and taste to various food products, contributing to the overall sensory experience of the consumer.
Used in Fragrance and Flavor Development:
Cyclohexaneacetic acid, 2-ethylidene-, methyl ester, (Z)is employed in the development of new fragrances and flavors, where its unique scent characteristics can be blended with other compounds to create innovative and appealing products.

Check Digit Verification of cas no

The CAS Registry Mumber 90173-11-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,1,7 and 3 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 90173-11:
(7*9)+(6*0)+(5*1)+(4*7)+(3*3)+(2*1)+(1*1)=108
108 % 10 = 8
So 90173-11-8 is a valid CAS Registry Number.

90173-11-8Downstream Products

90173-11-8Relevant academic research and scientific papers

Vinylogous Wolff Rearrangement. 4. General Reaction of β,γ-Unsaturated α'-Diazo Ketones

Smith, Amos B.,Toder, Bruce H.,Branca, Stephen J.

, p. 3995 - 4001 (2007/10/02)

The preparation and vinylogous Wolff rearrangement (VWR) of some 21 acyclic and monocyclic β,γ-unsaturated α'-diazo ketones are described.The resulting γ,δ-unsaturated esters are summarized in Tables I-VI.The rearrangement is promoted by CuSO4, Cu(AcAc)2,

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