62518-65-4 Usage
Uses
Used in Fragrance Industry:
3-(m-tert-butylphenyl)-2-methylpropionaldehyde is used as a fragrance ingredient for its ability to impart a floral and citrus scent to perfumes, colognes, and other personal care products, enhancing their appeal and sensory experience.
Used in Flavoring Industry:
In the food and beverage sector, 3-(m-tert-butylphenyl)-2-methylpropionaldehyde is utilized as a flavoring agent to add a unique taste and aroma to products, contributing to their overall flavor profile and consumer enjoyment.
Used in Cleaning Products:
3-(m-tert-butylphenyl)-2-methylpropionaldehyde is employed in household and industrial cleaning products due to its antimicrobial properties, which help in maintaining hygiene and preventing the growth of harmful microorganisms.
Used in Antimicrobial Applications:
3-(m-tert-butylphenyl)-2-methylpropionaldehyde is used as an antimicrobial agent in various applications for its effectiveness in inhibiting the growth of bacteria and other microorganisms, ensuring cleanliness and safety in different settings.
Check Digit Verification of cas no
The CAS Registry Mumber 62518-65-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,5,1 and 8 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 62518-65:
(7*6)+(6*2)+(5*5)+(4*1)+(3*8)+(2*6)+(1*5)=124
124 % 10 = 4
So 62518-65-4 is a valid CAS Registry Number.
InChI:InChI=1/C14H20O/c1-11(10-15)8-12-6-5-7-13(9-12)14(2,3)4/h5-7,9-11H,8H2,1-4H3
62518-65-4Relevant academic research and scientific papers
Oxidative coupling of benzenes with α,β-unsaturated aldehydes by the Pd(OAc)2/molybdovanadophosphoric acid/O2 system
Yamada, Tomoyuki,Sakaguchi, Satoshi,Ishii, Yasutaka
, p. 5471 - 5474 (2008/04/18)
The oxidative coupling reaction of benzene with an α,β- unsaturated aldehyde was examined by the combined catalytic system of Pd(OAc)2 with molybdovanadophosphoric acid (HPMoV) under atmospheric dioxygen. Thus, the reaction of benzene with acrolein under dioxygen (1 atm) by the use of catalytic amounts of Pd(OAc)2 and H4PMo 11VO40·26H2O in the presence of dibenzoylmethane as a ligand in propionic acid at 90 °C for 1.5 h afforded cinnamaldehyde in 59% yield and β-phenylcinnamaldehyde in 5% yield. This catalytic system was extended to the direct oxidative coupling through the C-H bond activation of various arenes with acrolein and methacrolein.
