223473-36-7 Usage
Uses
Used in Pharmaceutical Industry:
(2R)-2-AMINO-2-CYCLOPENTYLETHAN-1-OL is used as an intermediate in the synthesis of pharmaceuticals for its versatile molecular structure and unique cyclopentyl group attached to a chiral carbon.
Used in Organic Compounds Synthesis:
(2R)-2-AMINO-2-CYCLOPENTYLETHAN-1-OL is used as a building block in the production of organic compounds due to its cyclic amine and primary alcohol properties.
Used in Organic Synthesis Research:
(2R)-2-AMINO-2-CYCLOPENTYLETHAN-1-OL is used as a valuable reagent in organic synthesis research for its stereochemical properties and functional groups.
Used in Medicinal Chemistry Research:
(2R)-2-AMINO-2-CYCLOPENTYLETHAN-1-OL is used in medicinal chemistry research for its potential applications in the development of new pharmaceuticals and organic compounds.
Check Digit Verification of cas no
The CAS Registry Mumber 223473-36-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,3,4,7 and 3 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 223473-36:
(8*2)+(7*2)+(6*3)+(5*4)+(4*7)+(3*3)+(2*3)+(1*6)=117
117 % 10 = 7
So 223473-36-7 is a valid CAS Registry Number.
223473-36-7Relevant academic research and scientific papers
New expedient route to both enantiomers of nonproteinogenic α-amino acid derivatives from the unsaturated 2-aza-bicyclo moiety
Alonso, Diego A.,Bertilsson, Sophie K.,Johnsson, Sandra Y.,Nordin, Sofia J. M.,Soedergren, Mikael J.,Andersson, Pher G.
, p. 2276 - 2280 (2007/10/03)
The influence of the reaction conditions on the catalytic hydrogenation of 2-aza-bicyclo hept-5-ene and oct-5-ene derivatives has been investigated. We found it possible to fully control the extent of allylic vs benzylic C-N hydrogenolysis by simple variations of H2 pressure and acidity of the reaction medium. The use of the reaction pathways was demonstrated by the selective preparation of four categories of optically active α-amino acid derivatives. The strategy was also extended to the synthesis of enantiopure α-amino ketones.
