60025-25-4 Usage
Uses
Used in Pharmaceutical Applications:
(S)-2-amino-3-cyclohexyl-propionic acid ethyl ester; hydrochloride is used as a pharmaceutical intermediate for the development of new drugs. Its unique structure and properties allow it to be a promising candidate for therapeutic applications.
Used in Laboratory Research:
In laboratory settings, (S)-2-amino-3-cyclohexyl-propionic acid ethyl ester; hydrochloride serves as a research tool for studying the effects and interactions of amino acid derivatives in biological systems. Its cyclohexyl group and hydrochloride salt form provide a basis for investigating its potential role in various biological processes and mechanisms.
Used in Drug Development:
(S)-2-amino-3-cyclohexyl-propionic acid ethyl ester; hydrochloride is utilized in the drug development process to explore its potential as a therapeutic agent. Its unique properties and increased water solubility due to the hydrochloride salt form make it a valuable compound for further investigation and development into effective treatments.
Check Digit Verification of cas no
The CAS Registry Mumber 60025-25-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,0,2 and 5 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 60025-25:
(7*6)+(6*0)+(5*0)+(4*2)+(3*5)+(2*2)+(1*5)=74
74 % 10 = 4
So 60025-25-4 is a valid CAS Registry Number.
60025-25-4Relevant academic research and scientific papers
Asymmetric construction of quaternary stereocenters: Synthesis of enantiopure amino acid-based tricyclic α,β-enones through an ipso-Friedel-Crafts/Michael addition cascade
Rodriguez-Solla, Humberto,Concellon, Carmen,Tuya, Paula,Garcia-Granda, Santiago,Diaz, M. Rosario
experimental part, p. 295 - 300 (2012/04/04)
An efficient reaction of the (2R,1′S)- or (2S,1′S)-N,N-bis(p- methoxybenzyl)-2-(1-aminoalkyl)epoxides, derived from α-amino acids, with boron trifluoride-phosphoric acid complex is described. This process affords highly elaborated enantiopure tricyclic α,β-enones in high yields, through an ipso-Friedel-Crafts/Michael addition cascade. Copyright
