4017-89-4 Usage
Description
[1R-(1alpha,3alpha,4alpha,6alpha)]-4,7,7-trimethylbicyclo[4.1.0]heptan-3-ol, commonly known as Isomenthol, is a bicyclic compound with a molecular formula of C10H18O. It is a colorless liquid characterized by a strong and minty odor. This versatile chemical is used in a variety of applications across different industries due to its unique properties.
Uses
Used in Flavors and Fragrances Industry:
Isomenthol is used as a key component in the production of flavors and fragrances, adding a refreshing and minty scent to various products. Its strong odor makes it a valuable addition to the formulation of perfumes, colognes, and other scented products.
Used in Pharmaceutical and Personal Care Products:
In the pharmaceutical industry, Isomenthol serves as a cooling agent in products designed to provide temporary relief from minor aches and pains. Its cooling effect also makes it a popular ingredient in personal care products, such as creams and lotions, that aim to soothe and refresh the skin.
Used in Food and Beverages Industry:
As a flavoring agent, Isomenthol is utilized in the food and beverage industry to enhance the taste of various products. Its minty flavor adds a refreshing twist to candies, chewing gums, and beverages, making it a popular choice for manufacturers looking to create unique and appealing flavors.
Used as a Topical Analgesic:
Isomenthol is also used as a topical analgesic to provide temporary relief from minor aches and pains. Its cooling effect helps to soothe and alleviate discomfort, making it a popular choice for over-the-counter pain relief products.
It is important to handle Isomenthol with care and follow proper safety precautions due to its potential hazards. Proper handling and storage are essential to ensure the safety of both the users and the environment.
Check Digit Verification of cas no
The CAS Registry Mumber 4017-89-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,0,1 and 7 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 4017-89:
(6*4)+(5*0)+(4*1)+(3*7)+(2*8)+(1*9)=74
74 % 10 = 4
So 4017-89-4 is a valid CAS Registry Number.
InChI:InChI=1/C10H18O/c1-6-4-7-8(5-9(6)11)10(7,2)3/h6-9,11H,4-5H2,1-3H3/t6-,7-,8+,9+/m1/s1
4017-89-4Relevant articles and documents
Regioselective Routes to Nucleophilic Optically Active 2- and 3-Carene Systems
Paquette, Leo A.,Ross, Robert J.,Shi, Yao-Jun
, p. 1589 - 1598 (2007/10/02)
Commercially available (+)-3-carene (4) is shown to be capable of efficient conversion to vinyl bromides 28, 46, and 49 and to vinyl stannane 44.All four compounds stem from (+)-3-norcaranone (23), an optically pure ketone best prepared by epoxidation of 4, followed by oxirane ring opening, acetylation, ozonolysis, and CrCl2-promoted reduction.The strong proclivity exhibited by 23 to enolize in the cyclopropyl carbinyl sense is used to advantage to gain entry to 28 and 44.Remarkably, the tosylhydrazone of (+)-3-norcaranone (45) is distinguished from its ketoneprogenitor 23 by its capacity for highly regioselective deprotonation from the alternative α-position.The crossover has made possible synthetic access to 46 and 49.Other chemistry of this class of compounds is also presented, inluding a route to 51, a vinyl bromide epimeric to 49.Especially relevant to future work in the ingenol area is the ability of these molecules to serve as nucleophiles.Several reactions involving 28 are provided as exemplary of this property.
Novel Method for Hydroboration of Olefins Using Electrolysis
Shundo, Ryushi,Matsubara, Yoshiharu,Nishiguchi, Ikuzo,Hirashima, Tsuneaki
, p. 2033 - 2036 (2007/10/02)
A first example of electrochemical hydroboration of olefins was found.Anodic oxidation of sodium borohydride in the presence of olefins in diglyme followed by conventional oxidation gave the corresponding alcohols regio- and stereoselectively in good yields.