824-13-5 Usage
Uses
Used in Pharmaceutical Synthesis:
1-Hydroxy-4-methylbicyclo[2.2.2]octane is used as a building block in the synthesis of various biologically active compounds and pharmaceuticals. Its unique ring structure and functional groups contribute to the development of new drugs with potential therapeutic applications.
Used in Fine Chemicals Production:
In the fine chemicals industry, 1-Hydroxy-4-methylbicyclo[2.2.2]octane serves as a key intermediate for the production of specialty chemicals. Its ability to participate in a range of chemical reactions allows for the creation of high-value products used in various applications.
Used in Polymer Production:
1-Hydroxy-4-methylbicyclo[2.2.2]octane has been studied for its potential use in the production of polymers. Its incorporation into polymer structures can lead to materials with novel properties and improved performance characteristics.
Used as a Chiral Auxiliary in Asymmetric Synthesis:
In asymmetric synthesis, 1-Hydroxy-4-methylbicyclo[2.2.2]octane is utilized as a chiral auxiliary. Its stereochemistry aids in the selective formation of enantiomers, which is crucial for the production of enantiomerically pure compounds with specific biological activities.
Safety Considerations:
Due to its flammable nature and potential health hazards, 1-Hydroxy-4-methylbicyclo[2.2.2]octane should be handled with care, adhering to proper safety protocols to minimize risks during its use in various applications.
Check Digit Verification of cas no
The CAS Registry Mumber 824-13-5 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 8,2 and 4 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 824-13:
(5*8)+(4*2)+(3*4)+(2*1)+(1*3)=65
65 % 10 = 5
So 824-13-5 is a valid CAS Registry Number.
824-13-5Relevant academic research and scientific papers
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
SYNTHESIS OF BRIDGEHEAD BICYCLOOCTANOLS
Kopecky, Jan,Smejkal, Jaroslav,Hanus, Vladimir
, p. 1370 - 1375 (2007/10/02)
The paper describes syntheses of bicyclooctan-1-ol, its 4-methyl and 4-phenyl derivatives, and bicyclooctane-1,4-diol.
