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108122-24-3

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108122-24-3 Usage

Description

2(1H)-Pyridinone,6-(1-piperazinyl)-(9CI) is a heterocyclic chemical compound that belongs to the class of pyridinones. It features a pyridine ring fused to a six-membered ring and is attached to a piperazine molecule. 2(1H)-Pyridinone,6-(1-piperazinyl)-(9CI) holds potential in the pharmaceutical domain due to its capacity to engage with several receptors within the central nervous system, positioning it as a promising candidate for the creation of novel drugs aimed at treating neurological disorders. Moreover, it has been scrutinized for its anticancer potential and its utility as a ligand in the synthesis of metal complexes. The distinctive structural attributes and prospective biological functions of 2(1H)-Pyridinone,6-(1-piperazinyl)-(9CI) render it a compelling subject for additional exploration and advancement in both the pharmaceutical and chemical sectors.

Uses

Used in Pharmaceutical Industry:
2(1H)-Pyridinone,6-(1-piperazinyl)-(9CI) is utilized as a prospective active pharmaceutical ingredient for the development of new drugs targeting neurological disorders. Its interaction with various central nervous system receptors makes it a candidate for treating such conditions.
Used in Anticancer Research:
In the field of oncology, 2(1H)-Pyridinone,6-(1-piperazinyl)-(9CI) is studied for its potential as an anticancer agent, given its ability to affect cellular processes that may be pivotal in controlling or preventing the proliferation of cancer cells.
Used in Chemical Synthesis:
2(1H)-Pyridinone,6-(1-piperazinyl)-(9CI) serves as a ligand in the synthesis of metal complexes, which can have applications in various areas such as catalysis, material science, and as potential therapeutic agents.
Used in Research and Development:
2(1H)-Pyridinone,6-(1-piperazinyl)-(9CI) is also used as a subject of research and development in both academic and industrial laboratories, given its unique structure and potential to yield new insights and applications in the chemical and pharmaceutical realms.

Check Digit Verification of cas no

The CAS Registry Mumber 108122-24-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,8,1,2 and 2 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 108122-24:
(8*1)+(7*0)+(6*8)+(5*1)+(4*2)+(3*2)+(2*2)+(1*4)=83
83 % 10 = 3
So 108122-24-3 is a valid CAS Registry Number.

108122-24-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-piperazin-1-yl-3H-pyridin-2-one

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

More Details:108122-24-3 SDS

108122-24-3Downstream Products

108122-24-3Relevant articles and documents

6-Alkoxy-N,N-disubstituted-2-pyridinamines as Anticonvulsant Agents

Pavia, Michael R.,Taylor, Charles P.,Hershenson, Fred M.,Lobbestael, Sandra J.

, p. 1210 - 1214 (2007/10/02)

The anticonvulsant effect of a series of 6-alkoxy-N,N-disubstituted-2-pyridinamines is described. An investigation was carried out to optimize the activity/side-effect ratio in this series of compounds. The most desirable profile was seen with 1-piperazine, 6, and this compound was selected for a more complete pharmacological evaluation. Overall, 6 has a pharmacological profile that is very similar to that of diphenylhydantoin (phenytoin). While nearly equipotent to phenytoin, animal studies suggest a fairly short duration of action. In addition, 6 exhibited some troublesome side effects including central nervous system depression and hypothermia.

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