115338-32-4 Usage
Uses
Used in Pharmaceutical Industry:
1-[2-METHOXYPHENYL]-4-[4-(2-PHTHALIMIDO)-BUTYL]PIPERAZINE HYDROCHLORIDE is used as a serotonin SR-1A antagonist for its ability to block the serotonin receptor, which can be beneficial in the treatment of various neurological and psychiatric disorders. Its antagonistic properties allow it to modulate the serotonin signaling pathways, potentially leading to improved therapeutic outcomes in conditions such as depression, anxiety, and other mood disorders.
Used in Research and Development:
In the field of research and development, 1-[2-METHOXYPHENYL]-4-[4-(2-PHTHALIMIDO)-BUTYL]PIPERAZINE HYDROCHLORIDE serves as a valuable tool for studying the role of serotonin receptors in various biological processes. Its potent antagonistic activity enables researchers to investigate the underlying mechanisms of serotonin-related disorders and develop novel therapeutic strategies targeting the serotonin system.
Used in Drug Delivery Systems:
Similar to gallotannin, 1-[2-METHOXYPHENYL]-4-[4-(2-PHTHALIMIDO)-BUTYL]PIPERAZINE HYDROCHLORIDE can also be incorporated into drug delivery systems to enhance its bioavailability, delivery, and therapeutic efficacy. By employing various organic and metallic nanoparticles as carriers, the compound can be more effectively targeted to specific cells or tissues, potentially improving its overall effectiveness in treating serotonin-related disorders.
Check Digit Verification of cas no
The CAS Registry Mumber 115338-32-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,5,3,3 and 8 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 115338-32:
(8*1)+(7*1)+(6*5)+(5*3)+(4*3)+(3*8)+(2*3)+(1*2)=104
104 % 10 = 4
So 115338-32-4 is a valid CAS Registry Number.
InChI:InChI=1/C23H27N3O3.BrH/c1-29-21-11-5-4-10-20(21)25-16-14-24(15-17-25)12-6-7-13-26-22(27)18-8-2-3-9-19(18)23(26)28;/h2-5,8-11H,6-7,12-17H2,1H3;1H
115338-32-4Relevant academic research and scientific papers
An efficient synthesis of aripiprazole, buspirone and NAN-190 by the reductive alkylation of amines procedure
Kowalski, Piotr,Jaskowska, Jolanta
experimental part, p. 81 - 85 (2012/04/10)
The reductive alkylation of amines procedure was applied for the synthesis of aripiprazole 1a, buspirone 1b, and NAN-190 1c. The reductive alkylation of amines procedure was applied for the synthesis of aripiprazole 1a, buspirone 1b, and NAN-190 1c. Copyright
