99341-77-2 Usage
Uses
Used in Flavor Industry:
FENCHYL ACETATE is used as a flavoring agent for its aromatic properties. It is commonly used to add a unique and pleasant taste to various food and beverage products.
Used in Fragrance Industry:
FENCHYL ACETATE is used as a fragrance ingredient for its distinct and appealing scent. It is often incorporated into perfumes, colognes, and other scented products to provide a long-lasting and pleasant aroma.
Used in Aromatherapy:
FENCHYL ACETATE is used in aromatherapy for its potential therapeutic benefits. Its calming and soothing properties may help to reduce stress and anxiety, promote relaxation, and improve overall well-being.
Used in Cosmetics and Personal Care Products:
FENCHYL ACETATE is used as a key ingredient in various cosmetics and personal care products, such as lotions, creams, and shampoos, for its pleasant scent and potential skin conditioning properties.
Used in Pharmaceutical Industry:
FENCHYL ACETATE may also have potential applications in the pharmaceutical industry, such as in the development of new drugs or as a carrier for drug delivery systems. However, more research is needed to fully understand its potential uses and benefits in this field.
Preparation
By acetylation of fenchyl alcohol (Arctander, 1969).
Check Digit Verification of cas no
The CAS Registry Mumber 99341-77-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,9,3,4 and 1 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 99341-77:
(7*9)+(6*9)+(5*3)+(4*4)+(3*1)+(2*7)+(1*7)=172
172 % 10 = 2
So 99341-77-2 is a valid CAS Registry Number.
InChI:InChI=1/C12H20O2/c1-8(13)14-10-11(2,3)9-5-6-12(10,4)7-9/h9-10H,5-7H2,1-4H3/t9-,10?,12+/m0/s1
99341-77-2Relevant academic research and scientific papers
1,3,3-Trimethylbicyclo[2.2.1]heptan-2-endo-ol in Nucleophilic Substitution Reactions
Koval'skaya,Kozlov
, p. 1925 - 1927 (2007/10/03)
1,3,3-Trimethylbicyclo[2.2.1]heptan-2-endo-ol (fenchol) reacts with acetonitrile in the presence of sulfuric acid to selectively form an isofenchane derivative - N-acetyl-1,5,5-trimethylbicyclo[2.2.1]heptan-2-exo-amine as a result of nucleophilic addition at the most accessible carbon atom of a nonclassical 1,3,3-trimethylbicyclo[2.2.1]heptyl cation. The H2SO4-catalyzed reaction with acetic acid results in exclusive formation of 1,3,3-trimethylbicyclo[2.2.1]hept-2-exo-yl acetate, implying an SN2 reaction mechanism.
Rearrangement of Pinane Derivatives. Part 8. Deamination of 2αH-Pinan-3α-ylamine
Giddings, Rodney M.,Jones-Parry, Richard,Salmon, J. Roger,Whittaker, David
, p. 725 - 728 (2007/10/02)
Solvolysis of 2αH-pinan-3α-yl toluene-p-sulphonate has been shown to proceed with concomitant 1,2-hydride shift to give the pinan-2-yl carbocation.Contrary to earlier reports, this species reacts normally to give, in good yield, pinan-2-yl substitution products.In contrast the pinan-3-ylamines react via a similar route, but give much smaller amounts of pinan-2-yl products.The usual reasons for differences between solvolysis and deamination (i.e. the intermediacy of diazonium ions and/or high-energy ions) can be discounted, and possible reasons for the differences in behaviour are discussed.
