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2-Isobutyl-4-methyl-acetophenon, also known as 2-isobutyl-4-methylphenyl methyl ketone, is an organic compound with the chemical formula C12H16O. It is a colorless to pale yellow liquid with a strong, sweet, and floral odor. This ketone is widely used in the fragrance industry as a fixative and modifier, particularly in the formulation of perfumes, soaps, and cosmetics. It is also employed as a flavoring agent in food and beverages, imparting a fruity, apple-like taste. The compound is synthesized through various chemical reactions, such as the Friedel-Crafts acylation of toluene with isobutyl acetyl chloride. Due to its chemical structure, 2-isobutyl-4-methyl-acetophenon exhibits low toxicity and is considered safe for use in consumer products.

7315-79-9

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7315-79-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7315-79-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,3,1 and 5 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 7315-79:
(6*7)+(5*3)+(4*1)+(3*5)+(2*7)+(1*9)=99
99 % 10 = 9
So 7315-79-9 is a valid CAS Registry Number.

7315-79-9Downstream Products

7315-79-9Relevant academic research and scientific papers

Chelate-assisted oxidative coupling reaction of arylamides and unactivated alkenes: Mechanistic evidence for vinyl C-H bond activation promoted by an electrophilic ruthenium hydride catalyst

Kwon, Ki-Hyeok,Lee, Do W.,Yi, Chae S.

scheme or table, p. 5748 - 5750 (2011/02/23)

The cationic ruthenium hydride complex [(η6-C 6H6)(PCy3)(CO)RuH]+BF 4- was found to be a highly regioselective catalyst for the oxidative C-H coupling reaction of aryl-substituted amides and unactivated alkenes to give o-alkenylamide products. The kinetic and spectroscopic analyses support a mechanism involving a rapid vinyl C-H activation followed by a rate-limiting C-C bond formation step.

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