173340-22-2 Usage
Description
(4S)-4-(aminomethyl)-1-[(1R)-1-phenylethyl]pyrrolidin-2-one is a pyrrolidinone derivative with the molecular formula C14H20N2O. It is a chiral compound characterized by a 4S configuration and features a pyrrolidinone ring with an aminomethyl and a phenylethyl group attached. (4S)-4-(aminomethyl)-1-[(1R)-1-phenylethyl]pyrrolidin-2-one holds potential pharmaceutical applications and is a subject of interest for researchers in medicinal chemistry and drug development. It is crucial to handle and use this compound with proper safety measures and in accordance with regulations and guidelines for potentially hazardous chemicals.
Uses
Used in Pharmaceutical Applications:
(4S)-4-(aminomethyl)-1-[(1R)-1-phenylethyl]pyrrolidin-2-one is used as a compound of interest for its potential pharmaceutical applications due to its unique structure and chiral properties. It may contribute to the development of new drugs targeting various medical conditions.
Used in Medicinal Chemistry Research:
In the field of medicinal chemistry, (4S)-4-(aminomethyl)-1-[(1R)-1-phenylethyl]pyrrolidin-2-one is used as a key compound for studying its interactions with biological targets. Its structure may provide insights into the design of novel therapeutic agents.
Used in Drug Development:
(4S)-4-(aminomethyl)-1-[(1R)-1-phenylethyl]pyrrolidin-2-one is utilized in drug development as a starting point for the synthesis of new pharmaceuticals. Its chiral nature and unique functional groups make it a valuable building block for creating innovative and effective medications.
Used in Chemical Synthesis:
In the chemical synthesis industry, (4S)-4-(aminomethyl)-1-[(1R)-1-phenylethyl]pyrrolidin-2-one is used as a versatile intermediate for the creation of various complex organic molecules. Its unique structure allows for further functionalization and modification to produce a wide range of compounds with different applications.
Used in Chiral Compounds Research:
(4S)-4-(aminomethyl)-1-[(1R)-1-phenylethyl]pyrrolidin-2-one is employed in the study of chiral compounds, which are essential in understanding the stereochemistry of biologically active molecules. Its 4S configuration makes it a valuable tool for investigating the role of chirality in drug action and selectivity.
Used in Safety and Regulatory Compliance:
In the context of safety and regulatory compliance, (4S)-4-(aminomethyl)-1-[(1R)-1-phenylethyl]pyrrolidin-2-one serves as a reminder of the importance of handling potentially hazardous chemicals with care. It highlights the need for adherence to guidelines and regulations to ensure the safety of researchers and the environment.
Check Digit Verification of cas no
The CAS Registry Mumber 173340-22-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,3,3,4 and 0 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 173340-22:
(8*1)+(7*7)+(6*3)+(5*3)+(4*4)+(3*0)+(2*2)+(1*2)=112
112 % 10 = 2
So 173340-22-2 is a valid CAS Registry Number.
173340-22-2Relevant articles and documents
Adamantyl Iminocarbonyl-Substituted Pyrimidines As Inhibitors Of 11-Beta-HSD1 826
-
, (2011/05/03)
A compound of formula (I): and pharmaceutically-acceptable salts thereof, wherein the variable groups are defined within; their use in the inhibition of 11βHSD1, processes for making them and pharmaceutical compositions comprising them are also described
