215649-69-7 Usage
Description
2-(2-Hydroxyethylamino)-N-(4-chlorophenyl)acetamide is a chemical compound with the molecular formula C10H14ClNO2. It is an acetamide derivative featuring a 2-hydroxyethylamino group and a 4-chlorophenyl group. 2-(2-HYDROXYETHYLAMINO)-N-(4-CHLOROPHENYL)ACETAMIDE holds a broad spectrum of potential biological activities, making it a subject of interest in the fields of medicinal chemistry and drug development. Its specific applications and effects on biological systems are contingent upon its interactions with particular receptors or enzymatic pathways, and it may serve as a pharmaceutical agent or a research tool in pharmacology and biochemistry.
Uses
Used in Pharmaceutical Development:
2-(2-Hydroxyethylamino)-N-(4-chlorophenyl)acetamide is used as a pharmaceutical agent for its potential therapeutic effects. 2-(2-HYDROXYETHYLAMINO)-N-(4-CHLOROPHENYL)ACETAMIDE's unique structure allows it to interact with specific biological targets, which may lead to the development of new treatments for various diseases and conditions.
Used in Research Applications:
In the field of pharmacology, 2-(2-Hydroxyethylamino)-N-(4-chlorophenyl)acetamide is utilized as a research tool to study the mechanisms of action of drugs and their interactions with biological systems. Its ability to modulate specific receptors or pathways can provide valuable insights into the development of novel therapeutic strategies.
Used in Biochemical Studies:
2-(2-Hydroxyethylamino)-N-(4-chlorophenyl)acetamide is employed in biochemical research to explore its effects on enzymatic pathways and other biological processes. Understanding how this compound interacts with enzymes and other biomolecules can contribute to the advancement of knowledge in biochemistry and related disciplines.
Used in Medicinal Chemistry:
In medicinal chemistry, 2-(2-Hydroxyethylamino)-N-(4-chlorophenyl)acetamide is used to design and synthesize new drug candidates. Its structural features can be modified to optimize its pharmacological properties, potentially leading to the discovery of more effective and safer medications.
Used in Drug Screening:
2-(2-Hydroxyethylamino)-N-(4-chlorophenyl)acetamide is utilized in drug screening processes to identify potential lead compounds for further development. Its diverse biological activities make it a valuable candidate for high-throughput screening assays, which can accelerate the drug discovery process.
Used in Drug Delivery Systems:
To enhance the bioavailability and therapeutic efficacy of 2-(2-Hydroxyethylamino)-N-(4-chlorophenyl)acetamide, it can be incorporated into various drug delivery systems. These systems can improve the compound's stability, solubility, and targeted delivery to specific tissues or cells, thereby increasing its potential as a pharmaceutical agent.
Check Digit Verification of cas no
The CAS Registry Mumber 215649-69-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,5,6,4 and 9 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 215649-69:
(8*2)+(7*1)+(6*5)+(5*6)+(4*4)+(3*9)+(2*6)+(1*9)=147
147 % 10 = 7
So 215649-69-7 is a valid CAS Registry Number.
215649-69-7Relevant articles and documents
Efficient synthesis of N-arylpiperazinones via a selective intramolecular Mitsunobu cyclodehydration
Weissman, Steven A.,Lewis, Stephanie,Askin, David,Volante,Reider, Paul J.
, p. 7459 - 7462 (2007/10/03)
A practical two pot synthesis of N-arylpiperazinones from the corresponding aniline is described. The key transformation is a selective intramolecular Mitsunobu cyclodehydration of an amidoalcohol intermediate. A series of N-arylpiperazinones were prepared in yields up to 89%.
