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132312-62-0

1-(pyridin-4-ylmethyl)pyrrolidin-2-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 132312-62-0 Structure

  • Basic information

    1. Product Name: 1-(pyridin-4-ylmethyl)pyrrolidin-2-one
    2. Synonyms: 1-(pyridin-4-ylmethyl)pyrrolidin-2-one;1-(4-pyridylmethyl)-2-pyrrolidinone;1-(4-pyridylmethyl)-2-pyrrolidone;1-(4-pyridylmethyl)pyrrolidin-2-one
    3. CAS NO:132312-62-0
    4. Molecular Formula: C10H12N2O
    5. Molecular Weight: 176.21508
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 132312-62-0.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 1-(pyridin-4-ylmethyl)pyrrolidin-2-one(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-(pyridin-4-ylmethyl)pyrrolidin-2-one(132312-62-0)
    11. EPA Substance Registry System: 1-(pyridin-4-ylmethyl)pyrrolidin-2-one(132312-62-0)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: IRRITANT
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 132312-62-0(Hazardous Substances Data)

132312-62-0 Usage

Chemical structure

P4MP2O consists of a pyrrolidin-2-one ring with a pyridine moiety attached to the carbon at position 1.

Classification

It is a heterocyclic compound.

Pharmaceutical applications

P4MP2O has potential pharmaceutical applications, particularly in the field of drug development.

GABA(A) receptor modulator

P4MP2O has been studied for its potential as a GABA(A) receptor positive allosteric modulator.

Neurological disorders

Due to its potential as a GABA(A) receptor modulator, P4MP2O could be useful in the treatment of certain neurological disorders.

Anti-inflammatory potential

The compound has been investigated for its potential as an anti-inflammatory agent.

Analgesic potential

P4MP2O has also been studied for its potential as an analgesic agent.

Research interest

Its unique structure and potential biological activities make P4MP2O an interesting target for further research and potential drug development.

Check Digit Verification of cas no

The CAS Registry Mumber 132312-62-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,2,3,1 and 2 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 132312-62:
(8*1)+(7*3)+(6*2)+(5*3)+(4*1)+(3*2)+(2*6)+(1*2)=80
80 % 10 = 0
So 132312-62-0 is a valid CAS Registry Number.

132312-62-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(Pyridin-4-ylmethyl)pyrrolidin-2-one

1.2 Other means of identification

Product number -
Other names 1-(4-pyridinylmethyl)-2-pyrrolidinone

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:132312-62-0 SDS

132312-62-0Relevant articles and documents

A novel and efficient synthesis of a tetra-substituted imidazole

Hayes,Hayes, Jerome F.,Mitchell,Mitchell, Michael B.,Procter,Procter, Carry

, p. 273 - 274 (2007/10/02)

A novel synthesis of a tetra-substituted imidazole is described. A key feature of the synthesis is the regioselective deprotonation of picolylpyrrolidinone 3 and the efficient reaction of this anion with an aryl nitrile to give the pyrrolidinoimidazole nu

Process for large-scale production of BMY 21502

-

, (2008/06/13)

An improved process, suitable for adaption to large-scale manufacture for synthesis of the cerebral function enhancing agent BMY 21502.

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