59671-45-3 Usage
Description
1-(1-hydroxycyclohexyl)-3,3-dimethylbutan-2-one, commonly known as heliotropin, is a synthetic organic compound characterized by its sweet, vanilla-like odor. It is widely recognized in the fragrance industry for its ability to add a gourmand or powdery note to perfumes and other scented products. Derived from cyclohexanone, this compound has a molecular formula of C12H22O2 and is deemed safe for use in cosmetics and personal care products.
Uses
Used in Fragrance Industry:
Heliotropin is used as a fragrance ingredient for its sweet, vanilla-like scent, adding a gourmand or powdery note to perfumes and other scented products. Its ability to enhance the overall aroma of these products makes it a valuable addition to the fragrance industry.
Used in Cosmetics and Personal Care Products:
Due to its safety for use in cosmetics and personal care products, heliotropin is also utilized as an ingredient in a variety of consumer products within these industries. Its pleasant odor and compatibility with other ingredients make it a popular choice for enhancing the scent and overall appeal of these products.
Check Digit Verification of cas no
The CAS Registry Mumber 59671-45-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,9,6,7 and 1 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 59671-45:
(7*5)+(6*9)+(5*6)+(4*7)+(3*1)+(2*4)+(1*5)=163
163 % 10 = 3
So 59671-45-3 is a valid CAS Registry Number.
59671-45-3Relevant articles and documents
Iron-mediated electrochemical reaction of α-chloroesters with carbonyl compounds
Durandetti, Muriel,Meignein, Clothilde,Perichon, Jacques
, p. 317 - 320 (2007/10/03)
(Matrix presented) Reformatsky-type reactions have been performed efficiently using an electroassisted iron-complex catalysis. Valuable product such as β-hydroxyesters, ketones or nitriles are thus prepared with high yields.
Reduction of Substituted Δ2-Isoxazolines. Synthesis of β-Hydroxy Acid Derivatives
Curran, Dennis P.,Scanga, Susan A.,Fenk, Christopher J.
, p. 3474 - 3478 (2007/10/02)
Three separate methods are reported for the formation of β-hydroxy acid derivatives from readily available substituted Δ2-isoxazolines.Cycloaddition of 2,2-dimethylpropanenitrile oxide with a variety of olefins followed by reductive cleavage produces α '-tert-butyl β-hydroxy ketones.These are cleaved to β-hydroxy tert-butyl esters by Baeyer-Villiger oxidation with peroxytrifluoroacetic acid.In the second approach, α ',β-dihydroxy ketones are generated via cycloaddition of olefins with the nitrile oxide generated from 2--2-methyl-1-nitropropane followed by reductive ring opening.Standard periodic acid cleavage gives β-hydroxy acids.Finally, 3-methoxy-substituted Δ2-isoxazolines, readily available via benzenesulfonylcarbonitrile oxide-olefin cycloaddition and methoxide displacement, are directly reduced to β-hydroxy esters.
