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2-(2-Methoxy-phenyl)-piperazine, also known as 2-methoxyphenylpiperazine, is a psychoactive chemical compound belonging to the class of piperazine derivatives. It functions as a partial agonist of the serotonin 5-HT1A and 5-HT2A receptors, exhibiting potential in the treatment of various psychiatric disorders.

65709-27-5

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65709-27-5 Usage

Uses

Used in Pharmaceutical Industry:
2-(2-Methoxy-phenyl)-piperazine is used as a therapeutic agent for its potential role in the treatment of psychiatric disorders such as depression, anxiety, and schizophrenia. Its agonistic effects on serotonin receptors contribute to its psychotropic properties, making it a subject of interest in pharmaceutical research and development.
Used in Research Applications:
In the scientific community, 2-(2-Methoxy-phenyl)-piperazine serves as a research chemical, aiding in the study of serotonin receptor mechanisms and their influence on mood and behavior. This helps researchers better understand the pathways involved in mental health conditions and develop more effective treatments.

Check Digit Verification of cas no

The CAS Registry Mumber 65709-27-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,7,0 and 9 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 65709-27:
(7*6)+(6*5)+(5*7)+(4*0)+(3*9)+(2*2)+(1*7)=145
145 % 10 = 5
So 65709-27-5 is a valid CAS Registry Number.
InChI:InChI=1/C11H16N2O/c1-14-11-5-3-2-4-9(11)10-8-12-6-7-13-10/h2-5,10,12-13H,6-8H2,1H3

65709-27-5 Well-known Company Product Price

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  • Alfa Aesar

  • (H26408)  2-(2-Methoxyphenyl)piperazine monohydrate, 95%   

  • 65709-27-5

  • 250mg

  • 3214.0CNY

  • Detail

65709-27-5SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(2-methoxyphenyl)piperazine

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
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More Details:65709-27-5 SDS

65709-27-5Downstream Products

65709-27-5Relevant academic research and scientific papers

Discovery of novel 2-(3-phenylpiperazin-1-yl)-pyrimidin-4-ones as glycogen synthase kinase-3β inhibitors

Usui, Yoshihiro,Uehara, Fumiaki,Hiki, Shinsuke,Watanabe, Kazutoshi,Tanaka, Hiroshi,Shouda, Aya,Yokoshima, Satoshi,Aritomo, Keiichi,Adachi, Takashi,Fukunaga, Kenji,Sunada, Shinji,Nabeno, Mika,Saito, Ken-Ichi,Eguchi, Jun-ichi,Yamagami, Keiji,Asano, Shouichi,Tanaka, Shinji,Yuki, Satoshi,Yoshii, Narihiko,Fujimura, Masatake,Horikawa, Takashi

, p. 3726 - 3732 (2017/07/27)

We herein describe the results of further evolution of glycogen synthase kinase (GSK)-3β inhibitors from our promising compounds containing a 2-phenylmorpholine moiety. Transformation of the morpholine moiety into a piperazine moiety resulted in potent GSK-3β inhibitors. SAR studies focused on the phenyl moiety revealed that a 4-fluoro-2-methoxy group afforded potent inhibitory activity toward GSK-3β. Based on docking studies, new hydrogen bonding between the nitrogen atom of the piperazine moiety and the oxygen atom of the main chain of Gln185 has been indicated, which may contribute to increased activity compared with that of the corresponding phenylmorpholine analogues. Effect of the stereochemistry of the phenylpiperazine moiety is also discussed.

2-Arylpiperazine derivatives and the preparation thereof

-

, (2008/06/13)

A process is provided for preparing 2-arylpiperazine derivatives and more particularly, 2-phenylpiperazine derivatives of the formula STR1 wherein R represents a group selected from the group consisting of a halogen atom, a lower alkyl group (having carbon atoms of 1 to about 8, preferably 1 to 4), a lower alkoxy group (having carbon atoms of 1 to about 8, preferably 1 to 4), a nitro group, a cyano group, a benzyloxy group, a hydroxy group and when n is 2 R is a methylenedioxy group, and n represents 1, 2 or 3.

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