6848-93-7 Usage
General Description
4-Acetyl-4-methylcyclohexanone is a chemical compound with the molecular formula C9H14O2. It is a ketone, meaning it contains a carbonyl group (C=O) bonded to two carbon atoms. 4-Acetyl-4-methylcyclohexanone is used as a reagent in organic synthesis and can undergo various chemical reactions to produce other compounds. It is commonly used in the pharmaceutical and perfume industries as an intermediate in the production of drugs and fragrances. 4-Acetyl-4-methylcyclohexanone has a pleasant, fruity odor and is considered to be relatively stable under normal conditions. It is important to handle this chemical with care and follow proper safety precautions when working with it in a laboratory setting.
Check Digit Verification of cas no
The CAS Registry Mumber 6848-93-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,8,4 and 8 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 6848-93:
(6*6)+(5*8)+(4*4)+(3*8)+(2*9)+(1*3)=137
137 % 10 = 7
So 6848-93-7 is a valid CAS Registry Number.
InChI:InChI=1/C9H14O2/c1-7(10)9(2)5-3-8(11)4-6-9/h3-6H2,1-2H3
6848-93-7Relevant articles and documents
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
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