575467-47-9 Usage
Description
(2E)-1-[(2S)-2-(pyrrolidin-1-ylmethyl)pyrrolidin-1-yl]-3-[4-(trifluoromethyl)phenyl]prop-2-en-1-one is a complex organic chemical compound characterized by a molecular formula of C23H27F3N2O. It features two pyrrolidine rings, a trifluoromethylphenyl group, and a propenone moiety. (2E)-1-[(2S)-2-(pyrrolidin-1-ylmethyl)pyrrolidin-1-yl]-3-[4-(trifluoromethyl)phenyl]prop-2-en-1-one is frequently utilized in pharmaceutical research and development due to its potential biological activity and its role as a starting material for the synthesis of various drugs. Its specific uses and applications can vary across different fields of study, but it is recognized for its pharmacological properties that make it a valuable asset to researchers in the medical and pharmaceutical industries.
Uses
Used in Pharmaceutical Research and Development:
(2E)-1-[(2S)-2-(pyrrolidin-1-ylmethyl)pyrrolidin-1-yl]-3-[4-(trifluoromethyl)phenyl]prop-2-en-1-one is used as a starting material for the synthesis of various drugs, particularly in the pharmaceutical industry. Its unique structure and potential biological activity make it a promising candidate for the development of new therapeutic agents.
Used in Drug Synthesis:
In the field of medicinal chemistry, (2E)-1-[(2S)-2-(pyrrolidin-1-ylmethyl)pyrrolidin-1-yl]-3-[4-(trifluoromethyl)phenyl]prop-2-en-1-one is employed as a key intermediate in the synthesis of pharmaceutical compounds. Its presence in the molecular structure can contribute to the desired pharmacological properties of the final drug product.
Used in Biological Activity Studies:
(2E)-1-[(2S)-2-(pyrrolidin-1-ylmethyl)pyrrolidin-1-yl]-3-[4-(trifluoromethyl)phenyl]prop-2-en-1-one is also used in biological research to study its potential effects on various biological systems. This can include testing its interactions with different types of cells, enzymes, or receptors, which can provide insights into its therapeutic potential and possible applications in medicine.
Used in Drug Design and Optimization:
In the process of drug design, (2E)-1-[(2S)-2-(pyrrolidin-1-ylmethyl)pyrrolidin-1-yl]-3-[4-(trifluoromethyl)phenyl]prop-2-en-1-one serves as a valuable component for the development of new pharmaceutical agents. Its structural features can be modified and optimized to enhance the compound's efficacy, selectivity, and safety profile in the treatment of various diseases and conditions.
Used in Medicinal Chemistry Education:
Furthermore, (2E)-1-[(2S)-2-(pyrrolidin-1-ylmethyl)pyrrolidin-1-yl]-3-[4-(trifluoromethyl)phenyl]prop-2-en-1-one can be utilized as a teaching tool in medicinal chemistry education. It provides students with a real-world example of a complex organic molecule that is relevant to the pharmaceutical industry, helping them understand the principles of drug design, synthesis, and pharmacological evaluation.
Check Digit Verification of cas no
The CAS Registry Mumber 575467-47-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,7,5,4,6 and 7 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 575467-47:
(8*5)+(7*7)+(6*5)+(5*4)+(4*6)+(3*7)+(2*4)+(1*7)=199
199 % 10 = 9
So 575467-47-9 is a valid CAS Registry Number.
575467-47-9Relevant articles and documents
Cinnamic amides of (S)-2-(aminomethyl)pyrrolidines are potent H3 antagonists
Peschke, Bernd,Bak, Sonja,Hohlweg, Rolf,Pettersson, Ingrid,Frolund Refsgaard, Hanne Hoffmann,Viuff, Dorthe,Rimvall, Karin
, p. 2603 - 2616 (2007/10/03)
New imidazole-free H3 antagonists have been found in a series of cinnamic amides of (S)-(aminomethyl)pyrrolidines. The influence of the substituent on the aromatic moiety on the potency and the inhibition of three cytochrome P450 subtypes are also described.
