1197-54-2 Usage
Uses
Used in Chemical Reactions:
(4-Amino-cyclohexyl)-acetic acid is used as a reactant in various chemical reactions due to its amino and acid groups, which allow it to participate in a wide range of processes.
Used in Pharmaceutical Industry:
(4-Amino-cyclohexyl)-acetic acid is used as a building block for the synthesis of pharmaceutical compounds, leveraging its unique structure to create new drugs with potential therapeutic applications.
Used in Research and Development:
(4-Amino-cyclohexyl)-acetic acid is used as a research compound for studying its chemical properties and potential interactions with other molecules, which can lead to the discovery of new applications and uses in various industries.
Used in Material Science:
(4-Amino-cyclohexyl)-acetic acid is used as a component in the development of new materials, such as polymers and composites, where its unique structure can contribute to improved properties and performance.
Check Digit Verification of cas no
The CAS Registry Mumber 1197-54-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,1,9 and 7 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1197-54:
(6*1)+(5*1)+(4*9)+(3*7)+(2*5)+(1*4)=82
82 % 10 = 2
So 1197-54-2 is a valid CAS Registry Number.
InChI:InChI=1/C8H15NO2/c9-7-3-1-6(2-4-7)5-8(10)11/h6-7H,1-5,9H2,(H,10,11)
1197-54-2Relevant academic research and scientific papers
PROCESS FOR THE PREPARATION OF TRANS 4-AMINO-CYCLOHEXYL ACETIC ACID ETHYL ESTER HCL
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Page/Page column 2, (2011/12/12)
The invention relates to a process for the preparation of trans 4-amino-cyclohexil ethyl acetate HCl wherein d) hydrogenating 4-nitrophenyl acetic acid in a protic solvent at a temperature between 40-50° C. in the presence of Pd/C under 0.1-0.6 bar overpressure, and e) further hydrogenating the 4-aminophenyl acetic acid obtained in situ in step a) at a temperature between 50-60° C. under 1-4 bar overpressures, then f) heating to reflux the 4-aminocyclohexil acetic acid obtained in step b) for 1-3 hours in hydrochloric ethanol, and if desired after removing the solvent acetonitrile was added to the residue obtained and distilled off.
Aminopyrimidines with high affinity for both serotonin and dopamine receptors
Wustrow, David,Belliotti, Thomas,Glase, Shelly,Kesten, Suzanne Ross,Johnson, Don,Colbry, Norman,Rubin, Ronald,Blackburn, Anthony,Akunne, Hyacinth,Corbin, Ann,Duff Davis,Georgic, Lynn,Whetzel, Steven,Zoski, Kim,Heffner, Thomas,Pugsley, Thomas,Wise, Lawrence
, p. 760 - 771 (2007/10/03)
A series of {4-[2-(4-arylpiperazin-1-yl)alkyl]cyclohexyl}pyrimidin-2- ylamines was prepared and found to have receptor binding affinity for D2 and D3 dopamine (DA) receptors and serotonin 5-HT1A receptors. The structural contributions to D2/D3 and 5-HT1A
