3506-88-5 Usage
Uses
Used in Fragrance and Flavor Industry:
3-Benzyl-4-phenyl-2-butanone is used as a key ingredient in the fragrance and flavor industry for its pleasant and long-lasting scent. Its sweet, floral aroma contributes to the creation of various fragrances and flavors in products such as perfumes, soaps, and cosmetics.
Used in Antimicrobial Applications:
3-Benzyl-4-phenyl-2-butanone is used as an antimicrobial agent due to its ability to inhibit the growth of certain microorganisms. This property makes it suitable for use in various industrial applications where microbial control is essential, such as in the production of cosmetics and personal care products.
Used in Antioxidant Applications:
3-Benzyl-4-phenyl-2-butanone is also used as an antioxidant, which helps prevent the oxidation of other compounds in various industrial processes. Its antioxidant properties can be beneficial in extending the shelf life of products and maintaining their quality over time.
Check Digit Verification of cas no
The CAS Registry Mumber 3506-88-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,5,0 and 6 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 3506-88:
(6*3)+(5*5)+(4*0)+(3*6)+(2*8)+(1*8)=85
85 % 10 = 5
So 3506-88-5 is a valid CAS Registry Number.
InChI:InChI=1/C17H18O/c1-14(18)17(12-15-8-4-2-5-9-15)13-16-10-6-3-7-11-16/h2-11,17H,12-13H2,1H3
3506-88-5Relevant academic research and scientific papers
Catalyst-Free Decarboxylative Fluorination of Tertiary β-Keto Carboxylic Acids
Katada, Misaki,Kitahara, Kazumasa,Iwasa, Seiji,Shibatomi, Kazutaka
supporting information, p. 2408 - 2411 (2018/11/23)
Decarboxylative fluorination of tertiary β-keto carboxylic acids was performed using an electrophilic fluorinating reagent. The reaction proceeded in the absence of a catalyst or base to yield the corresponding α-fluoroketones with tertiary fluorocarbons in good to high yields. Considering that the α-fluorination of asymmetrical ketones often causes problems with the regioselectivity between the α- and α′-positions, this method could be a good alternative to the α-fluorination of simple ketones for the synthesis of tertiary fluoroketones.
Unusually stable silyl ketones with bowl-shaped tris(2,6-diphenylbenzyl)silyl group for various nucleophilic attacks and α-deprotonation
Shirakawa, Seiji,Komatsu, Naoki,Iwasaki, Atsuko,Maruoka, Keiji
, p. 577 - 579 (2007/10/03)
A newly designed, bowl-shaped tris(2,6-diphenylbenzyl)silyl (TDS) group can be successfully utilized as a highly effective shield of ketone carbonyls for various nucleophilic attacks and α-deprotonation. The high shielding effect of the bowl-shaped TDS mo
