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180161-17-5

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180161-17-5 Usage

General Description

4-(2-Fluorophenyl)piperidine is an organic chemical compound with the formula C11H14FN. It is a piperidine derivative with a fluorophenyl group attached to the fourth carbon atom. 4-(2-FLUOROPHENYL)PIPERIDINE is of interest in medicinal chemistry research as it has potential as a precursor in the synthesis of various pharmaceuticals, including antipsychotic and analgesic medications. It may also have applications in the development of new psychoactive substances. The fluorophenyl group in 4-(2-Fluorophenyl)piperidine contributes to its unique chemical and pharmacological properties, making it a valuable compound for further study and potential applications in drug development.

Check Digit Verification of cas no

The CAS Registry Mumber 180161-17-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,0,1,6 and 1 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 180161-17:
(8*1)+(7*8)+(6*0)+(5*1)+(4*6)+(3*1)+(2*1)+(1*7)=105
105 % 10 = 5
So 180161-17-5 is a valid CAS Registry Number.
InChI:InChI=1/C11H14FN/c12-11-4-2-1-3-10(11)9-5-7-13-8-6-9/h1-4,9,13H,5-8H2

180161-17-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(2-fluorophenyl)piperidine

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:180161-17-5 SDS

180161-17-5Relevant articles and documents

20-HETE FORMATION INHIBITORS

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Paragraph 0357-0360; 0393; 0394, (2020/08/23)

This disclosure provides novel heterocyclic compounds and methods for inhibiting the enzyme CYP4. Further disclosed methods include: a method of inhibiting the biosynthesis of 20-hydroxyeicosatetraenoic acid (20-HETE) in a subject in need thereof and a method of producing neuroprotection and decreased brain damage by preventing cerebral microvascular blood flow impairment and anti-oxidant mechanisms in a subject experiencing or having experienced an ischemic event.

Superacid-catalyzed preparation of aryl-substituted piperidines via dicationic electrophiles

Klumpp, Douglas A.,Beauchamp, Philip S.,Sanchez Jr., Gregorio V.,Aguirre, Sharon,De Leon, Sarah

, p. 5821 - 5823 (2007/10/03)

The electrophilic chemistry of 1,2,3,6-tetrahydropyridines has been studied in the Bronsted superacid, CF3SO3H (triflic acid). The 1,2,3,6-tetrahydropyridines react with arenes to give aryl-substituted piperidines. It is proposed tha

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