125269-17-2 Usage
Description
1-(2-[1-(4-BROMOPHENYL)-1H-TETRAAZOL-5-YL]VINYL)PIPERIDINE is a complex chemical compound characterized by a piperidine ring linked to a vinyl group, which is further connected to a tetraazol-5-yl ring substituted with a 4-bromophenyl group. 1-(2-[1-(4-BROMOPHENYL)-1H-TETRAAZOL-5-YL]VINYL)PIPERIDINE is known for its potential biological and pharmacological properties, making it a promising candidate for research and pharmaceutical applications.
Uses
Used in Pharmaceutical Research:
1-(2-[1-(4-BROMOPHENYL)-1H-TETRAAZOL-5-YL]VINYL)PIPERIDINE is used as a research compound for its potential to act as a ligand for certain receptors or enzymes. This application is due to its unique structure and properties that allow it to interact with specific biological targets, potentially leading to the development of new drugs for various medical conditions.
Used in Drug Development:
In the pharmaceutical industry, 1-(2-[1-(4-BROMOPHENYL)-1H-TETRAAZOL-5-YL]VINYL)PIPERIDINE is used as a key component in the development of new drugs. Its ability to modulate receptor or enzyme activity makes it a valuable tool for creating therapeutic agents that can address a range of medical conditions.
Used in Molecular Interaction Studies:
1-(2-[1-(4-BROMOPHENYL)-1H-TETRAAZOL-5-YL]VINYL)PIPERIDINE is also utilized in the study of molecular interactions and mechanisms within biological systems. Its unique structure enables researchers to gain insights into the complex processes that occur at the molecular level, which can contribute to a better understanding of various diseases and their potential treatments.
Overall, 1-(2-[1-(4-BROMOPHENYL)-1H-TETRAAZOL-5-YL]VINYL)PIPERIDINE is a versatile compound with significant potential in the fields of pharmaceutical research, drug development, and molecular interaction studies. Its diverse applications highlight the importance of continued research and exploration into its properties and potential uses.
Check Digit Verification of cas no
The CAS Registry Mumber 125269-17-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,5,2,6 and 9 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 125269-17:
(8*1)+(7*2)+(6*5)+(5*2)+(4*6)+(3*9)+(2*1)+(1*7)=122
122 % 10 = 2
So 125269-17-2 is a valid CAS Registry Number.
125269-17-2Relevant articles and documents
Tetrazole Compounds. 3. Modification of 1-Aryl-1H-tetrazole-5-acetaldehyde Enamines by Acid-Catalyzed Transamination
Fischer, G. W.
, p. 981 - 992 (2007/10/02)
The acid-catalyzed transamination of tetrazole-5-acetaldehyde enamines proves to be a useful synthetic method for preparing specially N-substituted enamines of this series not accessible directly from 3-chloro-propeniminium salts 3 and sodium azide.Thus,
