7779-54-6 Usage
Uses
Used in Fragrance Industry:
3-Nonanon-1-yl acetate is used as a fragrance ingredient for its herbaceous, fruity scent. It is commonly employed in the creation of perfumes, colognes, and other scented products to provide a fresh, natural aroma.
Used in Flavor Industry:
3-Nonanon-1-yl acetate is used as a flavoring agent for its fruity, green, and slightly woody taste. It is often utilized in the food and beverage industry to enhance the flavor of various products, such as candies, beverages, and baked goods.
Used in Cosmetics Industry:
3-Nonanon-1-yl acetate is used as an additive in the cosmetics industry to provide a pleasant scent to personal care products, such as lotions, creams, and shampoos. Its herbaceous, fruity odor adds a refreshing and natural fragrance to these products.
Used in Air Fresheners and Cleaning Products:
3-Nonanon-1-yl acetate is used as a scent component in air fresheners and cleaning products to provide a fresh, clean aroma. Its herbaceous, fruity scent helps to mask unpleasant odors and create a more pleasant environment.
Used in Aromatherapy:
3-Nonanon-1-yl acetate is used in aromatherapy for its potential mood-enhancing and stress-relieving properties. Its herbaceous, fruity scent is believed to have a calming and uplifting effect on the mind and body, making it a popular choice for use in aromatherapy practices.
Preparation
By condensation of methyl hexyl ketone with formaldehyde under mild alkaline conditions to yield β-ketol, which is
subsequently acetylated
Check Digit Verification of cas no
The CAS Registry Mumber 7779-54-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,7,7 and 9 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 7779-54:
(6*7)+(5*7)+(4*7)+(3*9)+(2*5)+(1*4)=146
146 % 10 = 6
So 7779-54-6 is a valid CAS Registry Number.
InChI:InChI=1/C11H20O3/c1-3-4-5-6-7-11(13)8-9-14-10(2)12/h3-9H2,1-2H3
7779-54-6Relevant academic research and scientific papers
Simple and clean synthesis of ketones from internal olefins using PdCl 2/N,N-dimethylacetamide catalyst system
Mitsudome, Takato,Yoshida, Syuhei,Tsubomoto, Yamato,Mizugaki, Tomoo,Jitsukawa, Koichiro,Kaneda, Kiyotomi
supporting information, p. 1596 - 1598 (2013/03/14)
A simple catalytic system consisting of PdCl2 and N,N-dimethylacetamide enabled clean and selective synthesis of ketones from internal olefins using molecular oxygen. Various functionalized internal olefins were directly and regioselectively oxidized; C atoms of CC bonds far from substituted moieties were preferably oxidized.
Ozonolysis of ricinolic acid derivatives and transformations of the ozonolysis products under barton reaction conditions
Ishmuratov,Kharisov,Shayakhmetova,Botsman,Shitikova,Tolstikov
, p. 643 - 649 (2008/02/01)
The possibility of functionalizing the alkyl part of ricinolic acid using the Barton reaction was investigated.
