1068-81-1 Usage
Uses
Used in Industrial Applications:
2,3-Heptanediol, 2-methylis used as a solvent for its ability to dissolve a wide range of substances, making it suitable for use in coatings, adhesives, and cleaning products. Its solubility properties contribute to the effectiveness and performance of these products.
Used in Flavor and Fragrance Production:
2,3-Heptanediol, 2-methylis used as a component in the production of flavors and fragrances due to its mild, sweet odor. This application takes advantage of its sensory characteristics to enhance the aroma of various consumer products.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 2,3-Heptanediol, 2-methylis used as an excipient or in the formulation of medications. Its properties may contribute to the stability, solubility, or delivery of active pharmaceutical ingredients.
Used in Cosmetic Industry:
2,3-Heptanediol, 2-methylis used in cosmetic products, where it may serve as a solvent, emollient, or humectant. Its mild properties make it suitable for use in personal care products, contributing to their texture, feel, and effectiveness.
Used as a Coupling Agent:
2,3-Heptanediol, 2-methylis used as a coupling agent in the formulation of various types of products. Its ability to bond with different materials makes it a valuable component in the creation of new and improved formulations across multiple industries.
Check Digit Verification of cas no
The CAS Registry Mumber 1068-81-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,0,6 and 8 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1068-81:
(6*1)+(5*0)+(4*6)+(3*8)+(2*8)+(1*1)=71
71 % 10 = 1
So 1068-81-1 is a valid CAS Registry Number.
1068-81-1Relevant academic research and scientific papers
Ruthenium Tetroxide Oxidation of Alkenes. A More Complete Picture
Albarella, Laura,Piccialli, Vincenzo,Sica, Donato,Smaldone, Dina
, p. 2442 - 2456 (2007/10/03)
The ruthenium tetroxide oxidation of some linear and cyclic alkenes, representatives of five substitution patterns, has been performed in acetone-water (5:1) solution at -70 deg C using stoichiometric ammounts of the oxidant.The main reaction products are 1,2-diols and/or α-ketols depending on the nature of the substrate little amounts of scission products, aldehydes and/or carboxylic acids, are also obtained.Generally 1,2-diols predominate over α-ketols except in the oxidation of (-)-α-pinene that afforded the α-ketol in 51percent yield while no trace of the corresponding 1,2-diol was detected.All reactions prceeded through the formation of unstable brownish precipitates, presumably the intermediate ruthenium (VI) esters, which easily decomposed during the work-up step.Results from oxidation of trans-7-tetradecene and cis and trans-11-tetradecenyl acetate indicated that the reaction was syn stereospecific.In some cases, 1,3-dioxolane products, formed by condensation of the 1,2-diol and the aldehyde materials, were also obtained among the reaction products.Their possible origin is briefly discussed.
