19830-09-2 Usage
Uses
Used in Organic Chemical Synthesis:
4-ACETYL-4-METHYLHEPTANEDIOIC ACID is utilized as a building block in the synthesis of organic chemicals, providing a foundation for the creation of a wide range of compounds with diverse properties and applications.
Used in Pharmaceutical Industry:
In the pharmaceutical sector, 4-ACETYL-4-METHYLHEPTANEDIOIC ACID is employed as a key intermediate in the development of new drugs, leveraging its unique structure to contribute to the medicinal properties of the final products.
Used as a Chelating Agent:
4-ACETYL-4-METHYLHEPTANEDIOIC ACID serves as a chelating agent, playing a crucial role in metal ion transport. Its ability to bind with metal ions makes it valuable in various chemical processes where metal ion management is essential.
Used as a Corrosion Inhibitor:
4-ACETYL-4-METHYLHEPTANEDIOIC ACID is also used as a corrosion inhibitor, protecting materials from the damaging effects of corrosive agents. Its application in this area is significant for industries that require protection of infrastructure and equipment from corrosion.
Used in Material Science:
4-ACETYL-4-METHYLHEPTANEDIOIC ACID has potential applications in the development of novel materials, where its unique structure can contribute to the creation of materials with enhanced properties.
Used as a Precursor for Specialty Polymers:
Furthermore, it is used as a precursor in the production of specialty polymers, where its chemical composition is key to achieving specific polymer characteristics for targeted applications.
Check Digit Verification of cas no
The CAS Registry Mumber 19830-09-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,8,3 and 0 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 19830-09:
(7*1)+(6*9)+(5*8)+(4*3)+(3*0)+(2*0)+(1*9)=122
122 % 10 = 2
So 19830-09-2 is a valid CAS Registry Number.
InChI:InChI=1/C10H16O5/c1-7(11)10(2,5-3-8(12)13)6-4-9(14)15/h3-6H2,1-2H3,(H,12,13)(H,14,15)/p-2
19830-09-2Relevant academic research and scientific papers
Synthesis of substituted tricyclo[5.3.1.04,9]undecan-2,6-dione from 4,4-disubstituted cyclohexanone enamines and methacryloyl chloride
Ahmed, M. Giasuddin,Ahmed, Syeda Asghari,Akhter, Kawsari,Tsuda, Yoshisuke,Hossain, M. Mahmun,Forsterling, F. Holger
, p. 1273 - 1283 (2007/10/03)
Morpholine enamines 4-acetyl-4-methyl-1-morpholinocyclohexene 4a, 4-acetyl-4-phenyl-1-morpholinocyclohexene 4b, and 4-acetyl-4-isopropenyl-1- morpholinocyclohexene 4c react with methacryloyl chloride to give 1,7-dimethyl-4(N-morpholino) tricyclo[5.3.1.0s
Transmission of Polar Substituent Effects Through the Bicyclooctane Ring System as Monitored by NMR Shifts: a 13C NMR Study of 4-Substituted-1-methylbicyclooctanes
Adcock, William,Abeywickrema, Anil N.,Iyer, V. Sankar,Kok, Gaik B.
, p. 213 - 220 (2007/10/02)
Carbon-13 substituent chemical shifts (SCS) are reported for the methyl group of a series of 4-substituted 1-methylbicyclooctanes covering a wide range of electronic substituent effects.Unlike the 13C SCS of the α-carbon centre in various unsaturat
The Synthesis of 1,4-Disubstituted Bicyclooctanes exhibiting Wide-range, Enantiotropic Nematic Phases
Gray, George W.,Kelly, Stephen M.
, p. 26 - 31 (2007/10/02)
The 1,4-disubstituted bicyclooctane ring has been incorporated in certain cyano-substituted systems to produce series of mesogens exhibiting wide-range nematic phases. 1-(4-Cyanophenyl)- and 1-(4'-cyanobiphenyl-4-yl)-4-n-alkylbicyclooctanes
