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4-((4-methylpiperazin-1-yl)methyl)picolinonitrile is a chemical compound with the molecular formula C14H18N4. It is a picolinonitrile derivative that contains a piperazine moiety. 4-((4-methylpiperazin-1-yl)methyl)picolinonitrile is recognized for its potential as a building block in the synthesis of pharmaceutical and agrochemical compounds, primarily due to its ability to act as a ligand in metal-mediated reactions. Its structure also endows it with potential biological activity, with research indicating its promise as an antipsychotic agent and its exploration for use in the development of therapeutic agents for a range of diseases.

1245646-64-3

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1245646-64-3 Usage

Uses

Used in Pharmaceutical Synthesis:
4-((4-methylpiperazin-1-yl)methyl)picolinonitrile is used as a key intermediate in the synthesis of various pharmaceutical compounds for its capacity to participate in metal-mediated reactions, which is crucial for the creation of new drugs with specific therapeutic properties.
Used in Agrochemical Development:
In the agrochemical industry, 4-((4-methylpiperazin-1-yl)methyl)picolinonitrile serves as a valuable component in the development of new agrochemicals, leveraging its chemical properties to enhance crop protection and management strategies.
Used in Antipsychotic Drug Research:
4-((4-methylpiperazin-1-yl)methyl)picolinonitrile is utilized as a potential antipsychotic agent in pharmaceutical research. Its structure and properties are under investigation for their ability to modulate neurotransmitter systems involved in psychotic disorders, offering a new avenue for treatment development.
Used in Therapeutic Agent Development for Various Diseases:
4-((4-methylpiperazin-1-yl)methyl)picolinonitrile is also under exploration for its potential application in the development of therapeutic agents for a variety of diseases. Its unique chemical structure may contribute to the creation of novel treatments that target specific biological pathways or mechanisms related to different disease conditions.

Check Digit Verification of cas no

The CAS Registry Mumber 1245646-64-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,4,5,6,4 and 6 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1245646-64:
(9*1)+(8*2)+(7*4)+(6*5)+(5*6)+(4*4)+(3*6)+(2*6)+(1*4)=163
163 % 10 = 3
So 1245646-64-3 is a valid CAS Registry Number.

1245646-64-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-[(4-methylpiperazin-1-yl)methyl]pyridine-2-carbonitrile

1.2 Other means of identification

Product number -
Other names 4-((4-methylpiperazin-1-yl)methyl)picolinonitrile

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:1245646-64-3 SDS

1245646-64-3Downstream Products

1245646-64-3Relevant academic research and scientific papers

Aminomethylation via cyclopalladated-ferrocenylimine-complexes-catalyzed Suzuki-Miyaura coupling of aryl halides with potassium N, N - dialkylaminomethyltrifluoroborates

Zou, Dapeng,Cui, Hongmeng,Qin, Lijin,Li, Jingya,Wu, Yangjie,Wu, Yusheng

scheme or table, p. 349 - 356 (2011/03/23)

Using cyclopalladated ferrocenylimine complexes (1-3 mol%) as catalysts, the Suzuki-Miyaura coupling of potassium N,N-dialkylaminomethyltrifluoroborates with aryl and heteroaryl halides were carried out in a 10:1 THF-H2O mixture at 80° in the presence of Cs2CO3 (3.0 equiv) as base, giving the desired cross-coupling products in 14-87% yields. A variety of potassium alkyltrifluoroborates were also examined. Georg Thieme Verlag Stuttgart New York.

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