4573-50-6 Usage
Description
(R)-6-(Isopropyl)-3-methylcyclohex-2-en-1-one is a light yellowish liquid with a herbaceous minty aroma. It has a high strength odor and is recommended to be smelled in a 1% solution or less.
Uses
Used in Flavor and Fragrance Industry:
(R)-6-(Isopropyl)-3-methylcyclohex-2-en-1-one is used as a flavoring agent for its herbaceous minty aroma. It is added to various food products and beverages to enhance their taste and aroma.
Used in Perfumery:
(R)-6-(Isopropyl)-3-methylcyclohex-2-en-1-one is used as a fragrance ingredient in perfumes and colognes. Its strong and distinctive aroma makes it a valuable component in creating unique and appealing scents.
Used in Aromatherapy:
(R)-6-(Isopropyl)-3-methylcyclohex-2-en-1-one is used in aromatherapy for its potential therapeutic benefits. Its herbaceous minty aroma can help create a calming and refreshing atmosphere, promoting relaxation and stress relief.
Used in Cosmetics and Personal Care Products:
(R)-6-(Isopropyl)-3-methylcyclohex-2-en-1-one is used as a scent component in cosmetics and personal care products such as soaps, shampoos, and lotions. Its pleasant aroma can enhance the overall sensory experience of these products.
Used in Insect Repellent Products:
(R)-6-(Isopropyl)-3-methylcyclohex-2-en-1-one has been found to have insect-repellent properties. It can be used in insect repellent products to help protect against biting insects and reduce the risk of insect-borne diseases.
Flammability and Explosibility
Notclassified
Check Digit Verification of cas no
The CAS Registry Mumber 4573-50-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,5,7 and 3 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 4573-50:
(6*4)+(5*5)+(4*7)+(3*3)+(2*5)+(1*0)=96
96 % 10 = 6
So 4573-50-6 is a valid CAS Registry Number.
InChI:InChI=1/C10H16O/c1-7(2)9-5-4-8(3)6-10(9)11/h6-7,9H,4-5H2,1-3H3/t9-/m1/s1
4573-50-6Relevant articles and documents
Synthesis of Cyclic Enones by Allyl-Palladium-Catalyzed α,β-Dehydrogenation
Huang, David,Zhao, Yizhou,Newhouse, Timothy R.
supporting information, p. 684 - 687 (2018/02/09)
The use of allyl-palladium catalysis for the one-step α,β-dehydrogenation of ketones via their zinc enolates is reported. The optimized protocol utilizes commercially available Zn(TMP)2 as base and diethyl allyl phosphate as oxidant. Notably, this transformation operates under salt-free conditions and tolerates a diverse scope of cycloalkanones.
Hydrolytic enantioselective protonation of cyclic dienyl esters and a β-diketone with chiral phase-transfer catalysts
Yamamoto, Eiji,Gokuden, Daichi,Nagai, Ayano,Kamachi, Takashi,Yoshizawa, Kazunari,Hamasaki, Akiyuki,Ishida, Tamao,Tokunaga, Makoto
supporting information, p. 6178 - 6181 (2013/02/25)
Hydrolytic enantioselective protonation of dienyl esters and a β-diketone catalyzed by phase-transfer catalysts are described. The latter reaction is the first example of an enantio-convergent retro-Claisen condensation. Corresponding various optically active α,β-unsaturated ketones having tertiary chiral centers adjacent to carbonyl groups were obtained in good to excellent yields and enantiomeric ratios (83-99%, up to 97.5:2.5 er).
The Lewis acid-catalyzed intramolecular asymmetric ene reaction using a chiral α-cyanovinylic sulfoxide as an enophile
Hiroi, Kunio,Umemura, Masayuki
, p. 1831 - 1840 (2007/10/02)
A chiral α-cyanovinylic sulfoxide served as an efficient chiral enophile in a Lewis acid-catalyzed intramolecular ene reaction. Use of diethylaluminum chloride as a catalyst provided extremely high stereoselectivity in the ene reaction. The stereochemistry of the ene reaction products were determined by chemical correlation and the NMR spectral analysis. A mechanistic pathway for the asymmetric induction is presented on the basis of the stereochemical results obtained.
