223473-31-2 Usage
Uses
Used in Pharmaceutical Research and Drug Development:
(2R)-cyclopentyl glycine ethyl ester is used as a building block for the synthesis of various bioactive molecules and drugs. Its unique structure allows it to be a valuable component in the creation of new pharmaceutical agents.
Used in Neurological Disorders and Psychiatric Conditions Treatment:
(2R)-cyclopentyl glycine ethyl ester is used as a therapeutic agent for the treatment of neurological disorders and psychiatric conditions. Its ability to modulate neurotransmitter activity in the brain makes it a promising candidate for addressing such health issues.
Used in Pain Management:
(2R)-cyclopentyl glycine ethyl ester is used as a potential medication for the treatment of pain. Its influence on neurotransmitter activity suggests that it could provide relief for individuals suffering from various types of pain.
Used in Anxiety Treatment:
(2R)-cyclopentyl glycine ethyl ester is used as a potential therapeutic agent for the treatment of anxiety. Its modulation of neurotransmitters in the brain may contribute to reducing anxiety symptoms in patients.
Used in Schizophrenia Treatment:
(2R)-cyclopentyl glycine ethyl ester is used as a potential medication for the treatment of schizophrenia. Its impact on neurotransmitter activity could help manage the symptoms associated with this psychiatric condition.
Check Digit Verification of cas no
The CAS Registry Mumber 223473-31-2 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 1 respectively.
Calculate Digit Verification of CAS Registry Number 223473-31:
(8*2)+(7*2)+(6*3)+(5*4)+(4*7)+(3*3)+(2*3)+(1*1)=112
112 % 10 = 2
So 223473-31-2 is a valid CAS Registry Number.
223473-31-2Relevant academic research and scientific papers
Alonso, Diego A.,Bertilsson, Sophie K.,Johnsson, Sandra Y.,Nordin, Sofia J. M.,Soedergren, Mikael J.,Andersson, Pher G.
, p. 2276 - 2280 (1999)
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.
