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(1S,3R,6R)-3-isopropyl-6-methyl-7-oxabicyclo[4.1.0]heptan-3-ol is a complex organic compound with a unique molecular structure. It is a chiral molecule, meaning it has a non-superimposable mirror image, and it is characterized by its specific stereochemistry, with the 1, 3, and 6 positions being occupied by different substituents: isopropyl, methyl, and hydroxyl groups, respectively. The compound features a seven-membered ring with an oxygen atom, which classifies it as a cyclic ether. The hydroxyl group at the 3-position indicates the presence of an alcohol functional group. (1S,3R,6R)-3-isopropyl-6-methyl-7-oxabicyclo[4.1.0]heptan-3-ol is likely to be found in the field of organic chemistry, potentially as an intermediate in the synthesis of more complex molecules or as a component in pharmaceuticals or fragrances, given its intricate structure and functional groups.

1845-68-7

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1845-68-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1845-68-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,8,4 and 5 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1845-68:
(6*1)+(5*8)+(4*4)+(3*5)+(2*6)+(1*8)=97
97 % 10 = 7
So 1845-68-7 is a valid CAS Registry Number.

1845-68-7Relevant academic research and scientific papers

A Novel Route to trans-Epoxidation of Terpinen-4-ol

Kozma, Erika,Cristea, Ioan,Mueller, Norbert

, p. 35 - 40 (2007/10/03)

Pure (1S,2R,4S)-1,2-epoxy-p-menthan-4-ol and (1R,2S,4R)-1,2-epoxy-p- menthan-4-ol (trans-epoxides of (4S)-terpinen-4-ol and (4R)-terpinen-4-ol) were prepared and certain reactions of these compounds with nucleophilic reagents were studied. It was shown th

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