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120351-93-1

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120351-93-1 Usage

Uses

2-(3-Fluorophenoxy)ethylamine acts as a reagent in the synthesis of neuronal nitric oxide synthase inhibitors with improved cellular permeability. Dimethyltetrahydropyrazino purinediones preparation as adenosine receptor antagonists.

Check Digit Verification of cas no

The CAS Registry Mumber 120351-93-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,0,3,5 and 1 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 120351-93:
(8*1)+(7*2)+(6*0)+(5*3)+(4*5)+(3*1)+(2*9)+(1*3)=81
81 % 10 = 1
So 120351-93-1 is a valid CAS Registry Number.
InChI:InChI=1/C8H10FNO/c9-7-2-1-3-8(6-7)11-5-4-10/h1-3,6H,4-5,10H2

120351-93-1 Well-known Company Product Price

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  • Alfa Aesar

  • (H51681)  2-(3-Fluorophenoxy)ethylamine hydrochloride, 98%   

  • 120351-93-1

  • 250mg

  • 603.0CNY

  • Detail
  • Alfa Aesar

  • (H51681)  2-(3-Fluorophenoxy)ethylamine hydrochloride, 98%   

  • 120351-93-1

  • 1g

  • 2156.0CNY

  • Detail
  • Alfa Aesar

  • (H50836)  2-(3-Fluorophenoxy)ethylamine   

  • 120351-93-1

  • 250mg

  • 765.0CNY

  • Detail
  • Alfa Aesar

  • (H50836)  2-(3-Fluorophenoxy)ethylamine   

  • 120351-93-1

  • 1g

  • 2757.0CNY

  • Detail

120351-93-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(3-Fluorophenoxy)ethylamine

1.2 Other means of identification

Product number -
Other names 2-(3-fluorophenoxy)ethanamine

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:120351-93-1 SDS

120351-93-1Relevant articles and documents

Discovery of Novel pERK1/2- or β-Arrestin-Preferring 5-HT1AReceptor-Biased Agonists: Diversified Therapeutic-like versus Side Effect Profile

Sniecikowska, Joanna,Gluch-Lutwin, Monika,Bucki, Adam,Wi?ckowska, Anna,Siwek, Agata,Jastrzebska-Wiesek, Magdalena,Partyka, Anna,Wilczyńska, Daria,Pytka, Karolina,Latacz, Gniewomir,Przejczowska-Pomierny, Katarzyna,Wyska, El?bieta,Weso?owska, Anna,Paw?owski, Maciej,Newman-Tancredi, Adrian,Kolaczkowski, Marcin

supporting information, p. 10946 - 10971 (2020/11/09)

Novel 1-(1-benzoylpiperidin-4-yl)methanamine derivatives with high affinity and selectivity for serotonin 5-HT1A receptors were obtained and tested in four functional assays: ERK1/2 phosphorylation, adenylyl cyclase inhibition, calcium mobilization, and β-arrestin recruitment. Compounds 44 and 56 (2-methylaminophenoxyethyl and 2-(1H-indol-4-yloxy)ethyl derivatives, respectively) were selected as biased agonists with highly differential "signaling fingerprints"that translated into distinct in vivo profiles. In vitro, 44 showed biased agonism for ERK1/2 phosphorylation and, in vivo, it preferentially exerted an antidepressant-like effect in the Porsolt forced swimming test in rats. In contrast, compound 56 exhibited a first-in-class profile: it preferentially and potently activated β-arrestin recruitment in vitro and potently elicited lower lip retraction in vivo, a component of "serotonergic syndrome". Both compounds showed promising developability properties. The presented 5-HT1A receptor-biased agonists, preferentially targeting various signaling pathways, have the potential to become drug candidates for distinct central nervous system pathologies and possessing accentuated therapeutic activity and reduced side effects.

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