53771-94-1 Usage
Description
(R)-2-(isopropyl)-5-methylcyclohexen-1-yl acetate, also known as isopulegol acetate, is a chemical compound that is widely recognized for its distinct floral, minty, and slightly fruity odor. It is a colorless liquid derived from menthol and is commonly found in essential oils from mint and other plants. Isopulegol acetate is valued for its pleasant aroma and flavor properties, making it a popular choice in the flavor and fragrance industry.
Uses
Used in Flavor and Fragrance Industry:
Isopulegol acetate is used as a key ingredient in the flavor and fragrance industry for its refreshing and cooling scent. It is particularly favored in the creation of perfumes, soaps, and cosmetics, where its unique aroma adds a pleasant and invigorating quality to the products.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, isopulegol acetate has potential applications due to its pleasant aroma and flavor properties. It can be utilized in the development of medications that require a more appealing taste or scent, enhancing patient compliance and overall experience with the medication.
Used in Food Industry:
The food industry also benefits from the use of isopulegol acetate, as it can be employed to enhance the flavor and aroma of various food products. Its refreshing and cooling scent makes it an ideal addition to products that require a more appealing taste or a boost in sensory appeal.
Check Digit Verification of cas no
The CAS Registry Mumber 53771-94-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,7,7 and 1 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 53771-94:
(7*5)+(6*3)+(5*7)+(4*7)+(3*1)+(2*9)+(1*4)=141
141 % 10 = 1
So 53771-94-1 is a valid CAS Registry Number.
InChI:InChI=1/C12H20O2/c1-8(2)11-6-5-9(3)7-12(11)14-10(4)13/h8-9H,5-7H2,1-4H3/t9-/m1/s1
53771-94-1Relevant articles and documents
Silica-catalysed and highly stereoselective convergent and nonconvergent rearrangements of menthone enol acetate epoxides: Easy access to the four α-hydroxymenthone stereoisomers
Tranchimand, Sylvain,Faure, Bruno,Naubron, Jean-Valere,Alphand, Veronique,Archelas, Alain,Iacazio, Gilles
experimental part, p. 4365 - 4372 (2012/09/07)
During a program dedicated to the biocatalytic access of structurally useful α-hydroxy ketones, we made the unexpected observation that epoxy enol acetates derived from (+)- and (-)-menthone stereoselectively rearranged on exposure to silica through a diastereoselective process, providing easy access to the complete set of α-hydroxymenthone stereoisomers. The absolute configurations of the four stereoisomers were unambiguously established by IR-VCD and X-ray diffraction, thus clarifying some literature discrepancy. Two of the four stereoisomers could also be obtained through astereoconvergent process, thus avoiding the inherent 50 % yield limitations of such diastereoselective reactions. A solvent-free version allowing an extremely rapid reaction ( 2 h) is also described. Finally, the observed diastereoselection was investigated by DFT calculations. Epoxy enol acetates derived from menthone unexpectedly rearranged diastereoselectively on exposure to silica, giving easy access to the complete set of α-hydroxymenthone stereoisomers. Two of the four stereoisomers were also available through a diastereoconvergent process. Finally, the observed stereoselection was investigated by DFT calculations. Copyright
The isomerization of menthol and the 3 enol acetats of 3-menthanone.
HUECKEL,JORDAN
, p. 563 - 568 (2007/10/14)
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