1280786-82-4 Usage
Description
1-(5-Bromo-2-fluorophenyl)pyrrolidine is a pyrrolidine derivative with the molecular formula C10H10BrFN. It features a bromine and fluorine substituent on the phenyl ring, which contributes to its unique chemical and physical properties. 1-(5-Bromo-2-fluorophenyl)pyrrolidine has garnered attention for its potential pharmaceutical properties, particularly as a dopamine receptor ligand. Its role in medicinal chemistry and drug development is of significant interest to researchers in the fields of organic synthesis and pharmaceutical science.
Uses
Used in Pharmaceutical Applications:
1-(5-Bromo-2-fluorophenyl)pyrrolidine is used as a dopamine receptor ligand for its potential role in the treatment of neurological disorders associated with dopamine dysregulation. Its interaction with dopamine receptors may offer therapeutic benefits in conditions such as Parkinson's disease, schizophrenia, and addiction.
Used in Medicinal Chemistry Research:
In the field of medicinal chemistry, 1-(5-Bromo-2-fluorophenyl)pyrrolidine serves as a valuable compound for studying the structure-activity relationship of dopamine receptor ligands. Its unique substitution pattern on the phenyl ring allows researchers to investigate the impact of bromine and fluorine atoms on the compound's binding affinity and selectivity for different dopamine receptor subtypes.
Used in Drug Development:
1-(5-Bromo-2-fluorophenyl)pyrrolidine is utilized in drug development as a lead compound for the discovery of novel therapeutic agents targeting the dopamine system. Its chemical properties and potential biological activities make it a promising candidate for further optimization and development into more potent and selective dopamine receptor modulators.
Used in Organic Synthesis:
In the realm of organic synthesis, 1-(5-Bromo-2-fluorophenyl)pyrrolidine is employed as a building block or intermediate for the synthesis of more complex molecules with potential applications in various industries, including pharmaceuticals, agrochemicals, and materials science. Its unique structural features and reactivity provide opportunities for the development of innovative synthetic routes and methodologies.
Check Digit Verification of cas no
The CAS Registry Mumber 1280786-82-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,8,0,7,8 and 6 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1280786-82:
(9*1)+(8*2)+(7*8)+(6*0)+(5*7)+(4*8)+(3*6)+(2*8)+(1*2)=184
184 % 10 = 4
So 1280786-82-4 is a valid CAS Registry Number.
1280786-82-4Relevant articles and documents
ANTI-AMYLOID COMPOUNDS AND METHODS
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Page/Page column 54-55, (2012/09/21)
Anti-amyloid compounds are provided along with methods of use thereof.
