38309-43-2 Usage
Uses
Used in Pharmaceutical Industry:
(1R,2R,6S)-6-methyl-7-oxabicyclo[4.1.0]heptan-2-ol is used as a therapeutic agent for its anti-inflammatory and analgesic properties. It is commonly found in products such as cough drops, throat lozenges, and topical analgesics to provide relief from pain and inflammation.
Used in Cosmetic Industry:
(1R,2R,6S)-6-methyl-7-oxabicyclo[4.1.0]heptan-2-ol is used as a cooling agent in cosmetics for its refreshing and soothing effects on the skin. It is often incorporated into products such as creams, lotions, and balms to provide a pleasant sensation and enhance the overall user experience.
Used in Food Industry:
(1R,2R,6S)-6-methyl-7-oxabicyclo[4.1.0]heptan-2-ol is used as a flavoring agent in food products to impart a minty taste and cooling sensation. It is commonly used in confectionery, beverages, and chewing gum to create a refreshing and enjoyable flavor profile.
Used in Pain Relief Applications:
(1R,2R,6S)-6-methyl-7-oxabicyclo[4.1.0]heptan-2-ol is used as a pain reliever for its mild anesthetic effects. It is particularly useful for relieving minor discomforts such as itching, sore muscles, and headaches when applied topically or consumed orally.
Used in Drug Delivery Systems:
(1R,2R,6S)-6-methyl-7-oxabicyclo[4.1.0]heptan-2-ol can be used in drug delivery systems to enhance the bioavailability and effectiveness of other active ingredients. Its cooling and soothing properties can improve the overall experience of using topical medications and transdermal patches.
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 academic research and scientific papers
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
Diastereoselective epoxidation of allylically substituted alkenes using metalloporphyrin catalysts
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Page/Page column 4, (2008/06/13)
Diastereoselective epoxidation of allylically substituted alkenes using metalloporphyrins as catalyst provides high trans-selectivities (i.e., trans-:cis-epoxide ratio). A diversity of cycloalkenes bearing different allylic substituents are shown to be efficiently epoxidized to afford the corresponding trans-epoxides with excellent trans-selectivities (up to >98%) and good yields (up to 99%). Acyclic allylic alkenes bearing different allylic substituents are efficiently epoxidized to afford the corresponding erythro-epoxides with good erythro-selectivities. The metalloporphyrin-catalyzed reactions exhibit up to 20 times higher trans-selectivities than the conventional method using m-chloroperoxybenzoic acid as oxidant.
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.
