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1,3-Dioxolo[4,5-g]quinoline, also known as 8CI and 9CI, is a heterocyclic organic compound characterized by a fused ring structure consisting of a quinoline ring (a tricyclic system with one benzene ring and two pyridine rings) and a dioxolo ring (a five-membered ring with two oxygen atoms). 1,3-Dioxolo[4,5-g]quinoline(8CI,9CI) is a member of the quinolines, a class of nitrogen-containing aromatic compounds with diverse applications in pharmaceuticals, agrochemicals, and materials science. The unique structure of 1,3-dioxolo[4,5-g]quinoline endows it with specific chemical and biological properties, making it a subject of interest in the synthesis of various derivatives for potential therapeutic and industrial applications.

269-51-2

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269-51-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 269-51-2 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 2,6 and 9 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 269-51:
(5*2)+(4*6)+(3*9)+(2*5)+(1*1)=72
72 % 10 = 2
So 269-51-2 is a valid CAS Registry Number.

269-51-2SDS

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 [1,3]dioxolo[4,5-g]quinoline

1.2 Other means of identification

Product number -
Other names [1,3]Dioxolo[4,5-g]chinolin

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:269-51-2 SDS

269-51-2Relevant academic research and scientific papers

Transformation of oximes of phenetyl ketone derivatives to quinolines and azaspirotrienones catalyzed by tetrabutylammonium perrhenate and trifluoromethanesulfonic acid

Kusama,Yamashita,Uchiyama,Narasaka

, p. 965 - 975 (2007/10/03)

Phenethyl ketone oximes are converted to quinolines by the treatment with tetrabutylammonium perrhenate, trifluoromethanesulfonic acid, and chloranil in refluxing 1,2-dichloroethane. Azaspirotrienones can be synthesized from p-hydroxyphenethyl or 3-(p-hydroxyphenyl)propyl ketone oximes by applying the above method. Thus prepared azaspirotrienones are converted to quinolines by acid treatment.

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