462632-54-8 Usage
General Description
3-[[[(1R,2R)-2-[[[[(1S)-1-[(Dimethylamino)carbonyl]-2,2-dimethylpropyl]amino]thioxomethyl]amino]cyclohexyl]imino]methyl]-5-(1,1-dimethylethyl)-4-hydroxyphenyl 2,2-dimethylpropanoate is a complex chemical compound with various functional groups and structural features. It contains a cyclohexyl ring, amino and hydroxy groups, and a thioxomethyl-imino moiety. The compound also includes a dimethylamino carbonyl group and a 2,2-dimethylpropanoate ester functionality. 3-[[[(1R,2R)-2-[[[[(1S)-1-[(Dimethylamino)carbonyl]-2,2-dimethylpropyl]amino]thioxomethyl]amino]cyclohexyl]imino]methyl]-5-(1,1-dimethylethyl)-4-hydroxyphenyl 2,2-dimethylpropanoate may have potential pharmacological properties or uses in chemical synthesis due to its structural complexity and diversity of functional groups. Further study and analysis are necessary to fully understand its chemical behavior and potential applications.
Check Digit Verification of cas no
The CAS Registry Mumber 462632-54-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,6,2,6,3 and 2 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 462632-54:
(8*4)+(7*6)+(6*2)+(5*6)+(4*3)+(3*2)+(2*5)+(1*4)=148
148 % 10 = 8
So 462632-54-8 is a valid CAS Registry Number.
462632-54-8Relevant articles and documents
Structure-based analysis and optimization of a highly enantioselective catalyst for the strecker reaction
Vachal, Petr,Jacobsen, Eric N.
, p. 10012 - 10014 (2002)
A mechanistic investigation of the asymmetric Strecker reaction catalyzed by a metal-free Schiff base catalyst was conducted. The active site of the catalyst, the relevant stereoisomer of the imine substrate, and the solution structure of the imine-catalyst complex were elucidated using a series of kinetics, structure-activity, and NMR experiments. An unusual bridging interaction between the imine and the urea hydrogens of the catalyst was identified and supported by computation. Rational optimization of catalyst structure based on the mechanistic insight led to an improved catalyst for the asymmetric Strecker reaction. Copyright
