61114-23-6 Usage
Description
[2-methoxy-4-[(E)-prop-1-enyl]phenyl] 3-methylbutanoate is a chemical compound with the molecular formula C15H20O3. It is an ester derived from 2-methoxy-4-[(E)-prop-1-enyl]phenol and 3-methylbutanoic acid, known for its fruity and floral aroma with a hint of spice.
Uses
Used in Fragrance Industry:
[2-methoxy-4-[(E)-prop-1-enyl]phenyl] 3-methylbutanoate is used as a flavoring agent and fragrance ingredient for its pleasant and versatile scent. It is popular in perfumes, colognes, and other scented products.
Used in Cosmetic Industry:
In the cosmetic industry, [2-methoxy-4-[(E)-prop-1-enyl]phenyl] 3-methylbutanoate is used as a scent additive for products such as soaps, shampoos, and detergents, enhancing their appeal with its fruity and floral aroma.
Used in Food Industry:
[2-methoxy-4-[(E)-prop-1-enyl]phenyl] 3-methylbutanoate is used as a flavoring agent in the food industry to impart its unique taste to various products, including baked goods, beverages, and confectionery.
Check Digit Verification of cas no
The CAS Registry Mumber 61114-23-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,1,1 and 4 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 61114-23:
(7*6)+(6*1)+(5*1)+(4*1)+(3*4)+(2*2)+(1*3)=76
76 % 10 = 6
So 61114-23-6 is a valid CAS Registry Number.
61114-23-6Relevant articles and documents
A general route for the stereoselective synthesis of (E)-(1-propenyl)phenyl esters by catalytic CC bond isomerization
Díaz-álvarez, Alba E.,Crochet, Pascale,Cadierno, Victorio
experimental part, p. 2611 - 2620 (2012/05/20)
A general and efficient procedure for the stereoselective synthesis of (E)-(1-propenyl)phenyl esters from readily accessible allylphenols has been developed. The process involves a two-step sequence consisting of the initial acylation of the allylphenols with an acid chloride, followed by catalytic CC bond isomerization in the resulting allylphenyl esters. The latter step was performed in methanol at 80 °C using catalytic amounts (0.5 mol %) of the commercially available bis(allyl)-ruthenium(IV) dimer [{RuCl(μ-Cl) (η3:η3-C10H16)} 2] (C10H16=2,7-dimethylocta-2,6-diene-1,8-diyl) . Reactions proceeded in high yields (68-93%) and short times (4-9 h) with complete E-selectivity.
