308358-04-5 Usage
Description
(R)-Pulegone Oxide, also known as the oxidized form of the monoterpene Pulegone, is a white solid compound that is commonly found in fragrant and flavoring agents. It is derived from Pulegone, which is a naturally occurring monoterpene that possesses a strong minty aroma and is widely used in the flavor and fragrance industry.
Uses
Used in Flavor and Fragrance Industry:
(R)-Pulegone Oxide is used as a flavoring agent for its strong minty aroma, adding a refreshing and cooling sensation to various food and beverage products. It is particularly popular in the production of chewing gum, toothpaste, and mouthwashes.
(R)-Pulegone Oxide is also used as a fragrance ingredient in the perfumery industry, where it contributes to the creation of complex and long-lasting scents. Its minty aroma can be used to enhance the overall scent profile of perfumes, colognes, and other fragrance products.
Used in Pharmaceutical Industry:
(R)-Pulegone Oxide has potential applications in the pharmaceutical industry due to its chemical properties and structural characteristics. It can be used as an intermediate in the synthesis of various drugs and active pharmaceutical ingredients (APIs), particularly those with analgesic, anti-inflammatory, or antispasmodic properties.
Used in Cosmetics Industry:
In the cosmetics industry, (R)-Pulegone Oxide can be used as an additive in the formulation of personal care products, such as creams, lotions, and shampoos. Its minty aroma can provide a cooling and refreshing sensation when applied to the skin or scalp, making it an attractive ingredient for products aimed at providing a soothing and invigorating experience.
Used in Research and Development:
(R)-Pulegone Oxide can be utilized in research and development for the study of its chemical properties, structural characteristics, and potential applications in various fields. It can serve as a model compound for understanding the behavior of other monoterpenes and their derivatives, as well as for exploring new methods of synthesis and modification.
Check Digit Verification of cas no
The CAS Registry Mumber 308358-04-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,0,8,3,5 and 8 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 308358-04:
(8*3)+(7*0)+(6*8)+(5*3)+(4*5)+(3*8)+(2*0)+(1*4)=135
135 % 10 = 5
So 308358-04-5 is a valid CAS Registry Number.
308358-04-5Relevant articles and documents
Total Synthesis of (-)-Carinatine A and (+)-Lycopladine A
Meng, Lingxing
, p. 7784 - 7789 (2016)
An efficient synthesis of two Lycopodium alkaloids, (-)-carinatine A and (+)-lycopladine A, is achieved in eight steps. The synthesis features an intramolecular aldol reaction for assembling the 6,5-fused ring system, a subsequent Tsuji-Trost allylation for generating a quarternary carbon center, and a 6π-electrocyclization to form the pyridine ring.
Efforts toward the synthesis of (+)-Lyconadin A
Karella, Satish,Raghavan, Sadagopan
, (2020/08/10)
Abstract: Synthetic efforts toward the synthesis of (+)-lyconadin A are described. B-Alkyl Suzuki coupling is utilized for combining 2-iodo cyclohexenone with the piperidine subunit. The piperidine subunit is derived from 5-bromo-3-nicotinic acid, and iod
The first asymmetric total synthesis of lycoposerramine-R
Ishida, Hiroaki,Kimura, Shinya,Kogure, Noriyuki,Kitajima, Mariko,Takayama, Hiromitsu
, p. 7762 - 7771 (2015/07/15)
The first asymmetric total synthesis of lycoposerramine-R, a Lycopodium alkaloid possessing a novel skeleton, was accomplished by a strategy featuring the stereoselective intramolecular aldol cyclization giving a cis-fused 5/6 bicyclic skeleton and a new method for the construction of the pyridone ring via the aza-Wittig reaction.
