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85803-63-0

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85803-63-0 Usage

General Description

2-(4-Methylpiperazin-1-yl)benzonitrile, also known as MPB, is a chemical compound that contains a piperazine ring and a benzonitrile group. It is commonly used in medicinal chemistry and drug discovery as a building block in the synthesis of pharmaceuticals. MPB is known to have affinity for serotonin and adrenergic receptors, making it a potential candidate for the development of new drugs for central nervous system disorders. It has shown promising results in preclinical studies for its potential as a therapeutic agent for conditions such as depression, anxiety, and schizophrenia. Additionally, MPB has been investigated for its potential to modulate neuronal activity and behavior, making it an important chemical for research in neuropharmacology and neuroscience.

Check Digit Verification of cas no

The CAS Registry Mumber 85803-63-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,5,8,0 and 3 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 85803-63:
(7*8)+(6*5)+(5*8)+(4*0)+(3*3)+(2*6)+(1*3)=150
150 % 10 = 0
So 85803-63-0 is a valid CAS Registry Number.
InChI:InChI=1/C12H15N3/c1-14-6-8-15(9-7-14)12-5-3-2-4-11(12)10-13/h2-5H,6-9H2,1H3

85803-63-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(4-Methylpiperazin-1-yl)benzonitrile

1.2 Other means of identification

Product number -
Other names 2-(4-METHYLPIPERAZIN-1-YL)BENZONITRILE

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 -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:85803-63-0 SDS

85803-63-0Relevant articles and documents

Synthesis and biological evaluation of N-hydroxyphenylacrylamides and N-hydroxypyridin-2-ylacrylamides as novel histone deacetylase inhibitors

Thaler, Florian,Colombo, Andrea,Mai, Antonello,Amici, Raffaella,Bigogno, Chiara,Boggio, Roberto,Cappa, Anna,Carrara, Simone,Cataudella, Tiziana,Fusar, Fulvia,Gianti, Eleonora,Di Ventimiglia, Samuele Joppolo,Moroni, Maurizio,Munari, Davide,Pain, Gilles,Regalia, Nickolas,Sartori, Luca,Vultaggio, Stefania,Dondio, Giulio,Gagliardi, Stefania,Minucci, Saverio,Mercurio, Ciro,Varasi, Mario

supporting information; experimental part, p. 822 - 839 (2010/07/05)

The histone deacetylases (HDACs) are able to regulate gene expression, and histone deacetylase inhibitors (HDACi) emerged as a new class of agents in the treatment of cancer as well as other human disorders such as neurodegenerative diseases. In the prese

Method of inhibiting neoplastic cells with imidazoquinazoline derivatives

-

, (2008/06/13)

A method for inhibiting neoplasia, particularly cancerous and precancerous lesions by exposing the affected cells to imidazoquinazoline derivatives.

Synthesis and biological properties of thiophene ring analogues of mianserin.

Watthey,Gavin,Desai,Finn,Rodebaugh,Patt

, p. 1116 - 1122 (2007/10/02)

The synthesis of two thiophene-containing analogues of mianserin, i.e., 1,2,3,4,10,13b-hexahydro-2-methylpiperazino[1,2-a]thieno[2, 3-c][1]benzazepine (2), and the corresponding [3,2-c] isomer (12) is described. The key step in the synthesis is the nucleo

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