1047-41-2 Usage
Uses
Used in Pharmaceutical Development:
4-(2-Chlorophenyl)-α-(phenoxymethyl)-1-piperazineethanol is used as a potential active pharmaceutical ingredient for the development of medications targeting various conditions. Its unique structure, including the chlorophenyl and piperazine components, may contribute to its efficacy in treating specific disorders, particularly those related to the central nervous system.
Used in Research and Development:
In the scientific community, 4-(2-Chlorophenyl)-α-(phenoxymethyl)-1-piperazineethanol serves as a subject of study for understanding its pharmacological activities and potential interactions with biological systems. Researchers use 4-(2-Chlorophenyl)-α-(phenoxymethyl)-1-piperazineethanol to explore its properties and evaluate its safety and efficacy in preclinical and clinical trials.
Used in Drug Design and Synthesis:
4-(2-Chlorophenyl)-α-(phenoxymethyl)-1-piperazineethanol is utilized in the design and synthesis of new drugs, leveraging its structural features to create novel therapeutic agents. Its potential to interact with specific biological targets makes it a valuable component in the development of innovative pharmaceuticals.
Check Digit Verification of cas no
The CAS Registry Mumber 1047-41-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,0,4 and 7 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1047-41:
(6*1)+(5*0)+(4*4)+(3*7)+(2*4)+(1*1)=52
52 % 10 = 2
So 1047-41-2 is a valid CAS Registry Number.
InChI:InChI=1/C19H23ClN2O2/c20-18-8-4-5-9-19(18)22-12-10-21(11-13-22)14-16(23)15-24-17-6-2-1-3-7-17/h1-9,16,23H,10-15H2
1047-41-2Relevant academic research and scientific papers
3-Tertiary amino-1-aryloxy- or aryl-propanes and -propan -2-ols and some related compounds
Gupta,Mukerji,Chatterjee,Rastogi,Anand,Dube,Sur Jr.,Mukerji,Srimal
, p. 241 - 246 (2007/10/04)
The synthesis and pharmacological activity of some 3 tertiary amino 1 aryloxy or 1 aryl, 1 thiophenoxy and 1 anilino propan 2 ols and propanes, particularly those derived from N phenylpiperazines are described. Effect of substituents (nature/position) on the phenyl ring, the phenoxy ring as well as alteration in the hydroxylic function vis a vis the structure activity relationships (SAR) are discussed. In general, the 1 aryloxy compounds have hypotensive activity this being more pronounced in those carrying an o substituent on the phenyl ring, while m and p substituted derivatives have their effect primarily on the CNS. Variations in the phenoxy moiety do not significantly alter the intrinsic activity. The 1 aryl compounds, on the other hand, have significant CNS activity, which is markedly affected by the substituents on the 1 aryl residue.
