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79421-39-9

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79421-39-9 Usage

General Description

The chemical 4-(1,4-dioxa-8-azaspiro[4.5]decan-8-yl)benzonitrile is a complex organic compound that contains a benzene ring, a nitrile group, and a spirocyclic ring system. The spirocyclic ring system is comprised of a six-membered oxygen-containing ring fused to an eight-membered nitrogen-containing ring, giving the molecule a unique and intricate structure. This chemical is of interest for its potential applications in medicinal chemistry and drug development, as spirocyclic compounds have been found to exhibit diverse biological activities. Additionally, its aromatic ring and nitrile functional group make it suitable for use in organic synthesis and as a building block for the synthesis of more complex molecules. The precise properties and potential uses of this compound would depend on its specific chemical and physical characteristics, which would need to be determined through experimental analysis.

Check Digit Verification of cas no

The CAS Registry Mumber 79421-39-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,9,4,2 and 1 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 79421-39:
(7*7)+(6*9)+(5*4)+(4*2)+(3*1)+(2*3)+(1*9)=149
149 % 10 = 9
So 79421-39-9 is a valid CAS Registry Number.

79421-39-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(1,4-dioxa-8-azaspiro[4.5]decan-8-yl)benzonitrile

1.2 Other means of identification

Product number -
Other names 4-(8-aza-1,4-dioxaspiro[4,5]dec-8-yl)benzonitrile

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:79421-39-9 SDS

79421-39-9Relevant articles and documents

ANTI-INFECTIVE COMPOUNDS

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Page/Page column 30, (2015/02/25)

The present invention relates to small molecule compounds and their use in the treatment of bacterial infections, in particular Tuberculosis.

An improved synthesis of N-aryl and N-heteroaryl substituted piperidones

Sch?n, Uwe,Messinger, Josef,Buckendahl,Prabhu,Konda

, p. 2519 - 2525 (2008/02/02)

An efficient Pd(0)-catalyzed protocol for the rapid and efficient preparation of N-aryl and N-heteroaryl substituted piperidones is described. The two step syntheses proceed with an overall yield of 50-70% using X-Phos as optimal ligand for the Pd(0)-cata

Two-directional photoinduced electron transfer in a trichromophoric system

Depaemelaere, Sigrid,De Schryver, Frans C.,Verhoeven, Jan W.

, p. 2109 - 2116 (2007/10/03)

Competition bewtween electron transfer via a through σ-bond and a through π-bond mechanism has been studied in 1-(4-cyanophenyl)-4-(cyanomethylene)piperidine. In this trichromophoric system designed in a configuration acceptor-donor-acceptor, where the do

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