133496-60-3 Usage
Uses
Used in Pharmaceutical Industry:
1(2H)-Naphthalenone, 3,4-dihydro-3-[[4-(2-methoxyphenyl)-1-piperazinyl]methyl]is used as a pharmaceutical intermediate for its potential pharmacological activity. 1(2H)-Naphthalenone,
3,4-dihydro-3-[[4-(2-methoxyphenyl)-1-piperazinyl]methyl]-'s unique structure allows it to be a promising candidate in the development of new drugs and therapies.
Used in Medicinal Research:
In the field of medicinal research, 1(2H)-Naphthalenone, 3,4-dihydro-3-[[4-(2-methoxyphenyl)-1-piperazinyl]methyl]is used as a compound with potential applications in drug discovery and design. Its complex structure and multiple functional groups make it a valuable tool for exploring new therapeutic approaches and targeting specific biological pathways.
Check Digit Verification of cas no
The CAS Registry Mumber 133496-60-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,3,4,9 and 6 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 133496-60:
(8*1)+(7*3)+(6*3)+(5*4)+(4*9)+(3*6)+(2*6)+(1*0)=133
133 % 10 = 3
So 133496-60-3 is a valid CAS Registry Number.
133496-60-3Relevant academic research and scientific papers
Chemoenzymatic synthesis and binding affinity of novel (R)- and (S)-3-aminomethyl-1-tetralones, potential atypical antipsychotics
Caro, Yolanda,Torrado, Maria,Masaguer, Christian F.,Ravina, Enrique,Padin, Fernando,Brea, Jose,Loza, Maria I.
, p. 585 - 589 (2007/10/03)
A series of (R)- and (S)-3-aminomethyl-1-tetralones, conformationally constrained analogues of haloperidol, have been obtained by enzymatic resolution of the corresponding racemic 3-hydroxymethyl-1-tetralones using Pseudomonas fluorescens lipase. Their bi
Synthesis and antidopaminergic activity of some 3-(aminomethyl)tetralones as analogues of butyrophenone
Cortizo,Santana,Ravina,Orallo,Fontenla,Castro,Calleja,De Ceballos
, p. 2242 - 2247 (2007/10/02)
Starting from β-benzoylpropionic acid we synthesized 3-(aminomethyl)tetralones in which the amino substituent was 4-(N-piperazinyl)-p-fluorobutyrophenone (14), 4-benzoylpiperidine (15), 4-hydroxy-4-phenylpiperidine (16) or 4-(o-methoxyphenyl)piperazine (1
