84604-51-3 Usage
General Description
(E)-2-methoxy-4-prop-1-enylphenyl isobutyrate is a chemical compound with the molecular formula C14H18O3. It is also known as 4-allyl-2-methoxyphenyl isobutyrate and is commonly used in the fragrance and flavor industry as a synthetic aromatic ingredient. (E)-2-methoxy-4-prop-1-enylphenyl isobutyrate is known for its floral and fruity scent, and is often used in perfumes, colognes, and other scented products. It is a clear, colorless liquid with a sweet, floral aroma and is considered safe for use in cosmetics and personal care products. It is important to note that this compound should be handled with care and precautions should be taken to avoid direct contact or ingestion.
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 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
, 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.
