84604-51-3 Usage
Uses
Used in Fragrance Industry:
(E)-2-methoxy-4-prop-1-enylphenyl isobutyrate is used as a synthetic aromatic ingredient for its floral and fruity scent, enhancing the overall fragrance profile of perfumes, colognes, and other scented products. Its distinct aroma adds a unique and appealing quality to these products, making it a valuable addition to the fragrance industry.
Used in Flavor Industry:
In addition to its application in the fragrance industry, (E)-2-methoxy-4-prop-1-enylphenyl isobutyrate is also employed as a flavoring agent. Its sweet, floral aroma contributes to the enhancement of various food and beverage products, providing a pleasant taste and aroma experience for consumers.
Used in Cosmetics and Personal Care Products:
(E)-2-methoxy-4-prop-1-enylphenyl isobutyrate is considered safe for use in cosmetics and personal care products, making it a suitable ingredient for these industries. Its floral and fruity scent adds a pleasant aroma to products such as lotions, creams, and shampoos, while also providing a visually appealing, clear, and colorless liquid form.
Check Digit Verification of cas no
The CAS Registry Mumber 84604-51-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,4,6,0 and 4 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 84604-51:
(7*8)+(6*4)+(5*6)+(4*0)+(3*4)+(2*5)+(1*1)=133
133 % 10 = 3
So 84604-51-3 is a valid CAS Registry Number.
InChI:InChI=1/C14H18O3/c1-5-6-11-7-8-12(13(9-11)16-4)17-14(15)10(2)3/h5-10H,1-4H3/b6-5+
84604-51-3Relevant academic research and scientific papers
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
, 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.
