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CAS

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136410-42-9

1-(4-fluorobenzyl)-5-(octyloxy)pyrrolidin-2-one is a chemical compound with a molecular formula C19H28FNO2. It is a pyrrolidin-2-one derivative featuring a 4-fluorobenzyl group and an octyloxy group attached to the pyrrolidin-2-one ring. 1-(4-fluorobenzyl)-5-(octyloxy)pyrrolidin-2-one may hold potential applications in the field of medicinal chemistry, particularly in the development of new pharmaceutical drugs. Its specific properties and potential uses would depend on further studies and research.

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  • 136410-42-9 Structure

  • Basic information

    1. Product Name: 1-(4-fluorobenzyl)-5-(octyloxy)pyrrolidin-2-one
    2. Synonyms:
    3. CAS NO:136410-42-9
    4. Molecular Formula: C19H28FNO2
    5. Molecular Weight: 321.4295
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 136410-42-9.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 455.5°C at 760 mmHg
    3. Flash Point: 229.3°C
    4. Appearance: N/A
    5. Density: 1.07g/cm3
    6. Vapor Pressure: 1.75E-08mmHg at 25°C
    7. Refractive Index: 1.518
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: 1-(4-fluorobenzyl)-5-(octyloxy)pyrrolidin-2-one(CAS DataBase Reference)
    11. NIST Chemistry Reference: 1-(4-fluorobenzyl)-5-(octyloxy)pyrrolidin-2-one(136410-42-9)
    12. EPA Substance Registry System: 1-(4-fluorobenzyl)-5-(octyloxy)pyrrolidin-2-one(136410-42-9)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 136410-42-9(Hazardous Substances Data)

136410-42-9 Usage

Uses

Used in Pharmaceutical Industry:
1-(4-fluorobenzyl)-5-(octyloxy)pyrrolidin-2-one is used as a chemical intermediate for the development of new pharmaceutical drugs. Its unique structure with a 4-fluorobenzyl group and an octyloxy group may contribute to its potential as a building block or modifier in the synthesis of novel drug candidates.
Used in Medicinal Chemistry Research:
1-(4-fluorobenzyl)-5-(octyloxy)pyrrolidin-2-one is used as a research compound to study its properties and explore its potential applications in medicinal chemistry. Further investigation may reveal its interactions with biological targets, which could lead to the discovery of new therapeutic agents or drug delivery systems.

Check Digit Verification of cas no

The CAS Registry Mumber 136410-42-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,6,4,1 and 0 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 136410-42:
(8*1)+(7*3)+(6*6)+(5*4)+(4*1)+(3*0)+(2*4)+(1*2)=99
99 % 10 = 9
So 136410-42-9 is a valid CAS Registry Number.

136410-42-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-[(4-fluorophenyl)methyl]-5-octoxypyrrolidin-2-one

1.2 Other means of identification

Product number -
Other names 2-Pyrrolidinone,1-((4-fluorophenyl)methyl)-5-(octyloxy)-,(+-)

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:136410-42-9 SDS

136410-42-9Downstream Products

136410-42-9Relevant articles and documents

Amnesia-reversal activity of a series of 5-alkoxy-1-arylcarbonyl-2-pyrrolidinones and 5-alkoxy-1-arylmethyl-2-pyrrolidinones

Toja, E,Gorini, C,Zirotti, C,Barzaghi, F,Galliani, G

, p. 415 - 422 (2007/10/02)

A series of 5-alkoxy-1-arylcarbonyl-2-pyrrolidinones (1-27) were prepared by condensation of arylcarbonyl chlorides with 5-alkoxy-2-pyrrolidinones in the presence of butyl lithium in tetrahydrofuran.Alkylation of these intermediates with substituted benzy

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