354539-62-1 Usage
Uses
Used in Food and Beverage Industry:
1-(4-Isobutoxyphenyl)propan-1-one is used as a flavoring agent for its sweet, fruity, and floral aroma, enhancing the taste and aroma of various food and beverage products.
Used in Perfumes and Cosmetics:
In the perfumery and cosmetics industry, 1-(4-Isobutoxyphenyl)propan-1-one is utilized as a fragrance ingredient, contributing to the creation of unique and appealing scents in perfumes, lotions, and other cosmetic products.
Used in Pharmaceutical Research:
1-(4-Isobutoxyphenyl)propan-1-one is studied for its potential pharmaceutical properties, particularly as an antibacterial and antifungal agent. Its effectiveness in combating certain bacteria and fungi is being investigated for possible applications in medicine and healthcare.
Used in Antimicrobial Applications:
As a compound with demonstrated antibacterial and antifungal properties, 1-(4-Isobutoxyphenyl)propan-1-one is being explored for use in antimicrobial applications, potentially serving as an active ingredient in products designed to inhibit the growth of harmful microorganisms.
Check Digit Verification of cas no
The CAS Registry Mumber 354539-62-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,5,4,5,3 and 9 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 354539-62:
(8*3)+(7*5)+(6*4)+(5*5)+(4*3)+(3*9)+(2*6)+(1*2)=161
161 % 10 = 1
So 354539-62-1 is a valid CAS Registry Number.
InChI:InChI=1/C13H18O2/c1-4-13(14)11-5-7-12(8-6-11)15-9-10(2)3/h5-8,10H,4,9H2,1-3H3
354539-62-1Relevant articles and documents
Catalytic Friedel-Crafts acylation of alkoxybenzenes mediated by aluminum hydrogensulfate in solution and solvent-free conditions
Salehi, Peyman,Khodaei, Mohammad Mehdi,Zolfigol, Mohammad Ali,Sirouszadeh, Sara
, p. 1863 - 1864 (2007/10/03)
Friedel-Crafts acylation of alkoxybenzenes was achieved efficiently by a reaction with aliphatic acid anhydrides in the presence of catalytic amounts of aluminum hydrogensulfate, Al(HSO4)3, in nitromethane and under solvent-free conditions. Alkylbenzenes and aryl halides, as well as aromatic anhydrides, remained intact under these conditions.
Catalytic Friedel-Crafts acylation of alkoxy benzenes by ferric hydrogensulfate
Salehi, Peyman,Khodaei, Mohammad Mahdi,Zolfigol, Mohammad Ali,Zeinoldini, Shahpour
, p. 1367 - 1373 (2007/10/03)
Friedel-Crafts acylation of alkoxy benzenes is achieved efficiently by reaction with aliphatic acid anhydrides in the presence of catalytic amounts of ferric hydrogensulfate, Fe(HSO4)3, in nitromethane. Alkyl benzenes and aryl halides, as well as aromatic anhydrides, remain intact under these conditions.
