1026692-54-5 Usage
General Description
2-(4-Methoxyphenyl)dihydro-2H-pyran-4(3H)-one is a chemical compound with a complex structure consisting of a 4-methoxyphenyl group attached to a dihydro-2H-pyran-4(3H)-one moiety. 2-(4-Methoxyphenyl)dihydro-2H-pyran-4(3H)-one belongs to the class of organic compounds known as benzenoids, which are characterized by benzene rings or ring systems containing benzene. It is potentially used in various scientific and industrial applications, however, specific information regarding its properties, uses, and safety is not widely available and should be referred from specific chemical databases or product manufacturers. Further research and testing may be necessary to fully understand its characteristics, potential benefits, and risks.
Check Digit Verification of cas no
The CAS Registry Mumber 1026692-54-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,2,6,6,9 and 2 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1026692-54:
(9*1)+(8*0)+(7*2)+(6*6)+(5*6)+(4*9)+(3*2)+(2*5)+(1*4)=145
145 % 10 = 5
So 1026692-54-5 is a valid CAS Registry Number.
1026692-54-5Relevant articles and documents
A novel self-terminated Prins strategy for the synthesis of tetrahydropyran-4-one derivatives and their behaviour in Fisher indole synthesis
Reddy, B. V. Subba,Anjum, S. Rehana,Sridhar
, p. 75133 - 75137 (2016/08/24)
A novel self-terminated Prins strategy has been developed for the synthesis of 2-substituted tetrahydropyran-4-one derivatives through a condensation of 3-(phenylthio)but-3-en-1-ol with carbonyl compounds in the presence of 5 mol% of Sc(OTf)3 u
Mechanistic analysis of oxidative C-H cleavages using inter- and intramolecular kinetic isotope effects
Jung, Hyung Hoon,Floreancig, Paul E.
experimental part, p. 10830 - 10836 (2010/02/28)
A series of monodeuterated benzylic and allylic ethers were subjected to oxidative carbon-hydrogen bond cleavage to determine the impact of structural variation on intramolecular kinetic isotope effects in DDQ-mediated cyclization reactions. These values
