80909-49-5 Usage
Uses
Used in Medicinal Chemistry:
(3S,4R)-1-benzyl-4-(4-fluorophenyl)pyrrolidine-3-carboxylic acid is used as a building block for the synthesis of bioactive compounds due to its structural features and the presence of the carboxylic acid group, which can be utilized in the formation of various chemical bonds and interactions with biological targets.
Used in Drug Development:
In the pharmaceutical industry, (3S,4R)-1-benzyl-4-(4-fluorophenyl)pyrrolidine-3-carboxylic acid is used as a precursor for the development of new drugs. Its chiral nature and functional groups may contribute to the creation of enantiomerically pure compounds with specific therapeutic effects, potentially leading to the discovery of novel medications with improved efficacy and selectivity.
Check Digit Verification of cas no
The CAS Registry Mumber 80909-49-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,0,9,0 and 9 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 80909-49:
(7*8)+(6*0)+(5*9)+(4*0)+(3*9)+(2*4)+(1*9)=145
145 % 10 = 5
So 80909-49-5 is a valid CAS Registry Number.
80909-49-5Relevant academic research and scientific papers
Tricyclic indeno-pyrrole derivatives as serotonin receptor modulators
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Page/Page column 16, (2008/06/13)
The present invention generally relates to a series of compounds, to pharmaceutical compositions containing the compounds, and to use of the compounds and compositions as therapeutic agents. More specifically, compounds of the present invention are tricyclic indeno-pyrrole compounds. These compounds are serotonin receptor (5-HT) ligands and are useful for treating diseases, disorders, and conditions wherein modulation of the activity of serotonin receptors (5-HT) is desired (e.g. anxiety, depression and obesity).
Synthesis of Phenyl- and Benzyl-Substituted Pyrrolidines and of a Piperidine by Intramolecular C-Alkylation. Synthons for Tricyclic Skeletons
Achini, Roland
, p. 2203 - 2218 (2007/10/02)
The construction of new or novelly functionalized annulated and bridged tricyclic compounds by two consecutive C,C-bond formations (a and b in 1a, Scheme 1) is described.In a first step, Chloroalkyl-substituted aminonitriles yielded pyrrolidines 8, 15a, 1
