936-92-5 Usage
Description
[1R-(1alpha,3beta,5beta,7alpha)]-3,8,8-trimethyl-4-oxatricyclo[5.1.0.03,5]octane, commonly known as rotundone, is a naturally occurring chemical compound found in various plants such as grapes and black pepper. It is characterized by its unique peppery aroma and taste, which contributes significantly to the sensory experience of red wines. Rotundone is recognized as a potent odorant with a low detection threshold, allowing it to be perceived even in small quantities.
Uses
Used in Food and Beverage Industry:
Rotundone is used as a flavor compound in the food and beverage industry, particularly in the production of wines. Its peppery aroma and taste enhance the overall sensory experience of the wine, making it an important ingredient in the creation of red wines.
Used in Fragrance Industry:
Due to its potent odorant properties and low detection threshold, rotundone can also be utilized in the fragrance industry to create unique and distinct scents for various products such as perfumes, colognes, and other scented items.
Used in Aromatherapy:
Rotundone's distinct peppery aroma can be employed in aromatherapy for its potential mood-enhancing and invigorating effects, contributing to a more relaxing and enjoyable experience for users.
Used in Research and Development:
The unique properties of rotundone make it an interesting compound for research and development in various fields, including the study of olfaction, flavor chemistry, and the development of new products in the food and beverage, fragrance, and aromatherapy industries.
Check Digit Verification of cas no
The CAS Registry Mumber 936-92-5 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 9,3 and 6 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 936-92:
(5*9)+(4*3)+(3*6)+(2*9)+(1*2)=95
95 % 10 = 5
So 936-92-5 is a valid CAS Registry Number.
936-92-5Relevant articles and documents
Carane amino alcohols as organocatalysts in asymmetric aldol reaction of isatin with acetone
Banina,Sudarikov,Nigmatov,Frolova,Slepukhin,Zlotin,Kutchin
, p. 293 - 296 (2017/07/11)
Carane-derived β-amino alcohols with amino and hydroxy groups at positions 3 and 4 differing in their mutual arrangement and configuration were synthesized. Their application as organocatalysts in the asymmetric aldol reaction of isatin with acetone allowed one to obtain adducts with up to 84% enantiomeric excess.
Switching the reaction pathways of electrochemically generated β-haloalkoxysulfonium ions - Synthesis of halohydrins and epoxides
Shimizu, Akihiro,Hayashi, Ryutaro,Ashikari, Yosuke,Nokami, Toshiki,Yoshida, Jun-Ichi
supporting information, p. 242 - 248 (2015/06/01)
β-Haloalkoxysulfonium ions generated by the reaction of electrogenerated Br+ and I+ ions stabilized by dimethyl sulfoxide (DMSO) reacted with sodium hydroxide and sodium methoxide to give the corresponding halohydrins and epoxides, respectively, whereas the treatment with triethylamine gave α-halocarbonyl compounds.
Syntheses of the optically active terpene hydroxyphenylselenides
Scianowski, Jacek,WeLniak, MirosLaw
experimental part, p. 1440 - 1447 (2010/03/24)
The optically active hydroxyphenylselenides derived from the p-menthane, carane, and pinane systems have been obtained. Two methods of hydroxyphenylselenides synthesis have been compared. The first method is based on the reaction of alkenes with N-(phenylseleno)succinimide in the presence of water, and the second from epoxides as a result of the reaction with sodium benzeneselenolate. The influence of the substrate structures on the composition of the obtained products has been demonstrated.
