6698-71-1 Usage
Description
1-(4-Methoxyphenoxy)-2-propanone, a chemical compound with the molecular formula C11H14O3, is a pale yellow liquid known for its solubility in organic solvents and its ability to act as a reagent in chemical reactions. The presence of methoxy and phenoxy groups in its structure makes it suitable for reactions involving organic synthesis and medicinal chemistry.
Uses
Used in Pharmaceutical Industry:
1-(4-Methoxyphenoxy)-2-propanone is used as an intermediate in the synthesis of various pharmaceutical drugs for its ability to facilitate organic reactions and contribute to the development of new medicinal compounds.
Used in Agrochemical Industry:
1-(4-Methoxyphenoxy)-2-propanone is used as an intermediate in the production of agrochemicals, playing a role in the synthesis of compounds that can be used in agriculture for pest control and crop protection.
Used in Flavor Industry:
1-(4-Methoxyphenoxy)-2-propanone is used as an intermediate in the creation of flavors, contributing to the development of unique taste profiles for food and beverage products.
Check Digit Verification of cas no
The CAS Registry Mumber 6698-71-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,6,9 and 8 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 6698-71:
(6*6)+(5*6)+(4*9)+(3*8)+(2*7)+(1*1)=141
141 % 10 = 1
So 6698-71-1 is a valid CAS Registry Number.
InChI:InChI=1/C10H12O3/c1-8(11)7-13-10-5-3-9(12-2)4-6-10/h3-6H,7H2,1-2H3
6698-71-1Relevant articles and documents
Selective aerobic oxidation of allyl phenyl ether to methyl ketone by palladium–polyoxometalate hybrid catalysts
Hong, Dachao,Kon, Yoshihiro,Shimoyama, Yoshihiro,Tamura, Satoru
, (2020/09/03)
In this study, we report that selective aerobic oxidation of allyl phenyl ethers is attained by a Pd catalyst/polyoxometalate hybrid system to yield corresponding methyl ketones in water-enriched acetonitrile. The Pd(OAc)2/H5PV2Mo10O40 system exhibits higher conversions and yields of corresponding methyl ketone by Wacker-type oxidation of allyl phenyl ether as compared with the conventional PdCl2/CuCl2 system. The higher yields are attributed to the efficient re-oxidation of Pd0 to Pd2+ by H5PV2Mo10O40 using O2 as an oxidant as evidenced by electrochemical measurements. A reduced species of H5PV2Mo10O40 by Pd0 during the catalytic oxidation is revealed by UV–vis spectral measurements. The use of PdCl2 in place of Pd(OAc)2 in combination with [PV2Mo10O40]5? bearing tetraalkylammonium counter cations has also exhibited comparable conversions and product yields in the Wacker-type oxidation of allyl phenyl ethers. Para-substituted allyl phenyl ether derivatives are successfully oxidized in the Pd catalyst/polyoxometalate system to yield corresponding methyl ketones. The initial rate of products of para-substituted methyl ketones depended on the electronic effect of the substituents in which allyl phenyl ethers with electron-donating groups have accelerated the initial rate in the Pd catalyst/polyoxometalate system.
