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"6-(3-chloro-4-fluorobenzoyl)-1-Oxa-6-azaspiro[2.5]octane-2-carbonitrile" is a complex organic compound with a molecular formula of C16H13ClFN2O2. It features a spiro[2.5]octane core, which is a type of spiro compound consisting of two rings sharing a common atom. In this case, the two rings are a six-membered azaspirane ring and a five-membered oxolane ring. The compound is further characterized by a 3-chloro-4-fluorobenzoyl group attached to the 6-position of the azaspirane ring, which introduces a halogenated aromatic moiety. Additionally, a carbonitrile group (-CN) is present at the 2-position of the azaspirane ring, contributing to the compound's reactivity and potential applications in chemical synthesis. This molecule's structure and properties make it a candidate for various applications in the pharmaceutical and chemical industries, particularly in the development of new drugs and other bioactive compounds.

448920-97-6

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448920-97-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 448920-97-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,4,8,9,2 and 0 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 448920-97:
(8*4)+(7*4)+(6*8)+(5*9)+(4*2)+(3*0)+(2*9)+(1*7)=186
186 % 10 = 6
So 448920-97-6 is a valid CAS Registry Number.

448920-97-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-(3-chloro-4-fluorobenzoyl)-2-cyano-1-oxa-6-azaspiro[2.5]octane

1.2 Other means of identification

Product number -
Other names 6-(3-Chloro-4-fluorobenzoyl)-1-oxa-6-azaspiro[2.5]octane-2-carbonitrile

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:448920-97-6 SDS

448920-97-6Relevant academic research and scientific papers

Novel Aryloxyethyl Derivatives of 1-(1-Benzoylpiperidin-4-yl)methanamine as the Extracellular Regulated Kinases 1/2 (ERK1/2) Phosphorylation-Preferring Serotonin 5-HT1A Receptor-Biased Agonists with Robust Antidepressant-like Activity

Sniecikowska, Joanna,Gluch-Lutwin, Monika,Bucki, Adam,Wieckowska, Anna,Siwek, Agata,Jastrzebska-Wiesek, Magdalena,Partyka, Anna,Wilczyńska, Daria,Pytka, Karolina,Pociecha, Krzysztof,Cios, Agnieszka,Wyska, Elzbieta,Wesolowska, Anna,Pawlowski, Maciej,Varney, Mark A.,Newman-Tancredi, Adrian,Kolaczkowski, Marcin

, p. 2750 - 2771 (2019/03/11)

Novel 1-(1-benzoylpiperidin-4-yl)methanamine derivatives were designed as "biased agonists" of serotonin 5-HT1A receptors. The compounds were tested in signal transduction assays (ERK1/2 phosphorylation, cAMP inhibition, Ca2+ mobiliz

Deuterium-Substituted Pyridin- And Pyrimidin-2-yl-Methylamine Compounds

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Paragraph 0310; 0311, (2018/04/14)

Described are deuterium-substituted pyridin- and pyrimidin-2-yl-methylamine compounds of structural Formula (I), which are agonists of 5-hydroxytryptamine receptors. Also described are pharmaceutical compositions comprising the deuterium-substituted pyridin- and pyrimidin-2-yl-methylamine compounds, and methods of use thereof.

Synthesis method and intermediates of pyridin-2-yl-methylamine

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Page 5, (2008/06/13)

The invention concerns a novel method for preparing pyridin-2-yl-methylamine derivatives by reducing amination of cyanohydrins.

Pyridylmethylamines polypyridine-2-yl-synthesis of the intermediate body,

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Page 12, (2008/06/13)

The invention concerns a novel method for preparing pyridin-2-yl-methylamine derivatives by reducing amination of cyanohydrins.

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