198422-64-9 Usage
Uses
Used in Medicinal Chemistry:
[(1S,2S)-2-hydroxycyclohexyl]CarbaMic acidphenylMethyl ester is used as a building block for the synthesis of new drugs or other biologically active molecules due to its unique structure and stereochemistry. Its potential applications in medicinal chemistry make it a valuable compound for further research and development.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, [(1S,2S)-2-hydroxycyclohexyl]CarbaMic acidphenylMethyl ester is used as a precursor for the development of novel therapeutic agents. Its complex structure and stereochemistry allow for the creation of new molecules with potential medicinal properties, contributing to the advancement of drug discovery and innovation.
Used in Chemical Research:
[(1S,2S)-2-hydroxycyclohexyl]CarbaMic acidphenylMethyl ester is also used in chemical research as a model compound to study the effects of stereochemistry on the biological activity of molecules. Understanding these effects can lead to the design of more effective and targeted drugs with fewer side effects.
Used in Drug Delivery Systems:
Similar to gallotannin, [(1S,2S)-2-hydroxycyclohexyl]CarbaMic acidphenylMethyl ester could be employed in the development of drug delivery systems. Its unique structure and properties may allow for the creation of innovative carriers for drug molecules, potentially improving their delivery, bioavailability, and therapeutic outcomes.
Check Digit Verification of cas no
The CAS Registry Mumber 198422-64-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,8,4,2 and 2 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 198422-64:
(8*1)+(7*9)+(6*8)+(5*4)+(4*2)+(3*2)+(2*6)+(1*4)=169
169 % 10 = 9
So 198422-64-9 is a valid CAS Registry Number.
198422-64-9Relevant academic research and scientific papers
Designing enzymatic resolution of amines
Takayama, Shuichi,Lee, Shelly T.,Hung, Shang-Cheng,Wong, Chi-Huey
, p. 127 - 128 (2007/10/03)
A new strategy, utilizing IR and mass spectrometry, has been developed to design appropriate reagents and reaction conditions for enantioselective enzymatic protection of amines with readily removable protecting groups.
Enzymatic resolution of (±)-trans-2-aminocyclohexanol and (±) trans-2-aminocyclopentanol
Maestro, Alicia,Astorga, Covadonga,Gotor, Vicente
, p. 3153 - 3159 (2007/10/03)
Candida antarctica lipase (CAL) catalyzes the resolution of (±)-trans-2-aminocyclohexanol by alkoxycarbonylation or acylation reactions. Besides, N-benzyloxycarbonyl derivatives of (±)-trans-2-aminocyclohexanol and (±)-trans-2-aminocyclopentanol are efficiently resolved through O-acylation by Pseudomonas cepacia lipase (PSL).
A General Method for the Separation of Enantiomeric trans-2-Substituted Cyclohexanols
Hoenig, Helmut,Seufer-Wasserthal, Peter
, p. 1137 - 1140 (2007/10/02)
An number of different racemic, trans-2-substituted cyclohexanols has been prepared in high optical purity by optical resolution of the respective 2'-substituted cyclohexyl butanoates with the aid of commercially available lipases.
