198422-64-9 Usage
General Description
[(1S,2S)-2-hydroxycyclohexyl]CarbaMic acidphenylMethyl ester is a chemical compound with a complex structure. It is a carbaMic acid ester that features a cyclohexyl ring with a hydroxyl group attached to it, as well as a phenyl group and a methyl ester. [(1S,2S)-2-hydroxycyclohexyl]CarbaMic acidphenylMethyl ester has potential applications in medicinal chemistry, as it could be used as a building block for the synthesis of new drugs or other biologically active molecules. Its stereochemistry, with the (1S,2S) configuration, is also an important feature that can impact its biological activity. Overall, [(1S,2S)-2-hydroxycyclohexyl]CarbaMic acidphenylMethyl ester is a versatile compound with interesting chemical properties and potential applications in various fields.
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 articles and documents
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.
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.
