93302-56-8 Usage
Description
(E)-1-(2,6,6-trimethyl-2-cyclohexen-1-yl)pent-1-en-3-one, with the molecular formula C13H22O, is a chemical compound that exists as a yellow liquid. It is characterized by a fruity and floral odor, which makes it a popular choice for use in the fragrance industry. (E)-1-(2,6,6-trimethyl-2-cyclohexen-1-yl)pent-1-en-3-one is also recognized for its potential anti-inflammatory and antioxidant properties, which extend its utility to skincare and pharmaceutical products. Moreover, it finds application in the food and beverage industry as a flavoring agent. While it is considered safe for use in low concentrations, caution is advised due to its flammable nature.
Uses
Used in Fragrance Industry:
(E)-1-(2,6,6-trimethyl-2-cyclohexen-1-yl)pent-1-en-3-one is used as a fragrance ingredient for its fruity and floral odor, contributing to the scent profiles of perfumes, soaps, and cosmetics.
Used in Skincare and Pharmaceutical Products:
In the skincare and pharmaceutical industries, (E)-1-(2,6,6-trimethyl-2-cyclohexen-1-yl)pent-1-en-3-one is used as an additive for its potential anti-inflammatory and antioxidant properties, which can be beneficial for various skin care formulations and medicinal applications.
Used in Food and Beverage Industry:
Within the food and beverage sector, (E)-1-(2,6,6-trimethyl-2-cyclohexen-1-yl)pent-1-en-3-one is utilized as a flavoring agent to enhance the taste and aroma of various products.
Check Digit Verification of cas no
The CAS Registry Mumber 93302-56-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,3,3,0 and 2 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 93302-56:
(7*9)+(6*3)+(5*3)+(4*0)+(3*2)+(2*5)+(1*6)=118
118 % 10 = 8
So 93302-56-8 is a valid CAS Registry Number.
InChI:InChI=1/C14H22O/c1-5-12(15)8-9-13-11(2)7-6-10-14(13,3)4/h7-9,13H,5-6,10H2,1-4H3/b9-8+
93302-56-8Relevant articles and documents
Photochemical transformations of terpenoids in the presence of cyclodextrins
Luzina,Tatarova,Korchagina,Salakhutdinov,Barkhash
, p. 183 - 193 (2007/10/03)
The effect of complexation of terpene compounds with cyclodextrins on photolysis depends on the type of cyclodextrin and on the structure of the initial substrates. In some cases, only a change in the reaction rate is observed; in other cases, the complexation results in allylic rearrangements, hydride and acyl shifts, and cyclization with the formation of four-, five-, and six-membered cycles, whereas only cis-trans isomerization reactions are observed in the absence of complexation.
