38309-43-2 Usage
General Description
The chemical (1R,2R,6S)-6-methyl-7-oxabicyclo[4.1.0]heptan-2-ol, also known as menthol, is a naturally occurring compound found in mint oils. It is commonly used in a variety of products including pharmaceuticals, cosmetics, and food. Menthol has a cooling sensation and is often used for its soothing properties, particularly in products such as cough drops, throat lozenges, and topical analgesics. It also has anti-inflammatory and analgesic properties, making it a popular ingredient in pain relief ointments and gels. Additionally, menthol has been found to have mild anesthetic effects, making it useful for relieving minor discomforts such as itching and sore muscles.
Check Digit Verification of cas no
The CAS Registry Mumber 38309-43-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,8,3,0 and 9 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 38309-43:
(7*3)+(6*8)+(5*3)+(4*0)+(3*9)+(2*4)+(1*3)=122
122 % 10 = 2
So 38309-43-2 is a valid CAS Registry Number.
38309-43-2Relevant articles and documents
Stereo- and regioselectivity in the P450-catalyzed oxidative tandem difunctionalization of 1-methylcyclohexene
Roiban, Gheorghe-Doru,Agudo, Rubén,Reetz, Manfred T.
, p. 5306 - 5311 (2013/07/05)
The selective partial oxidation of small non-functionalized molecules using biocatalysis based on P450 monooxygenases is known to be difficult due to the expected poor regio- and stereoselectivity, but in this study it was nevertheless attempted. 1-Methyl
Diastereoselectivity in the epoxidation of substituted cyclohexenes by dimethyldioxirane
Murray, Robert W.,Singh, Megh,Williams, Brian L.,Moncrieff, Hazel M.
, p. 1830 - 1841 (2007/10/03)
Three series of compounds based on the cyclohexene framework have been epoxidized by dimetbyldioxirane. A pronounced dependence of epoxide diastereoselectivity on substituent has been observed. In addition there is a solvent influence on this stereoselectivity. The results have been explained by invoking steric, H-bonding, and dipole - dipole influences on the epoxide stereochemistry.
