52263-19-1 Usage
Uses
Used in Pharmaceutical Industry:
Diethyl methyl(3-oxocyclohexyl)malonate is used as an intermediate in the synthesis of various pharmaceuticals for its versatile reactivity in organic reactions.
Used in Agrochemical Industry:
Diethyl methyl(3-oxocyclohexyl)malonate is used as an intermediate in the synthesis of various agrochemicals for its versatile reactivity in organic reactions.
Used in Flavors and Fragrances Industry:
Diethyl methyl(3-oxocyclohexyl)malonate is used as an intermediate in the production of flavors and fragrances for its versatile reactivity in organic reactions.
Used in Organic Compounds Synthesis:
Diethyl methyl(3-oxocyclohexyl)malonate is used as an intermediate in the synthesis of various organic compounds for its versatile reactivity in organic reactions.
Check Digit Verification of cas no
The CAS Registry Mumber 52263-19-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,2,2,6 and 3 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 52263-19:
(7*5)+(6*2)+(5*2)+(4*6)+(3*3)+(2*1)+(1*9)=101
101 % 10 = 1
So 52263-19-1 is a valid CAS Registry Number.
InChI:InChI=1/C14H22O5/c1-4-18-12(16)14(3,13(17)19-5-2)10-7-6-8-11(15)9-10/h10H,4-9H2,1-3H3
52263-19-1Relevant academic research and scientific papers
Highly efficient 1,4-addition of 1,3-diesters to conjugated enones by In/TMSCl
Lee, Phil Ho,Seomoon, Dong,Lee, Kooyeon,Heo, Yunkiu
, p. 2510 - 2513 (2007/10/03)
Organoindium reagents derived from indium and diethyl bromomalonates were added to a wide range of conjugated enones in a 1,4-fashion in the presence of TMSCl under mild conditions, and corresponding oxo-1,3-diesters were obtained in good to excellent yields.
Process of making 6-chloro-α-methyl-carbazole-2-acetic acid
-
, (2008/06/13)
The aromatization of (6-chloro-1,2,3,4-tetrahydro-2-carbazolyl)-methyl-malonic acid dialkyl ester, utilizing chlorine and subsequent conversion of the resulting product to 6-chloro-α-methyl-carbazole-2-acetic acid by hydrolysis and decarboxylation are described.
