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2217-31-4

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2217-31-4 Usage

General Description

3-Ethyl-2-hydroxyquinoline is a chemical compound with the molecular formula C13H13NO. It is a hydroxyquinoline derivative with a methyl group attached to the quinoline ring at the 3-position. 3-ETHYL-2-HYDROXYQUINOLINE has been studied for its potential pharmacological properties, including its antifungal, antibacterial, and antioxidant activities. It has also been explored for its potential applications in various industries, including the pharmaceutical and agricultural sectors. Additionally, 3-ethyl-2-hydroxyquinoline has been investigated for its potential role in the development of new materials and as a chelating agent in chemical processes.

Check Digit Verification of cas no

The CAS Registry Mumber 2217-31-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,2,1 and 7 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 2217-31:
(6*2)+(5*2)+(4*1)+(3*7)+(2*3)+(1*1)=54
54 % 10 = 4
So 2217-31-4 is a valid CAS Registry Number.
InChI:InChI=1/C11H11NO/c1-2-8-7-9-5-3-4-6-10(9)12-11(8)13/h3-7H,2H2,1H3,(H,12,13)

2217-31-4SDS

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 3-ethyl-1H-quinolin-2-one

1.2 Other means of identification

Product number -
Other names 3-ETHYL-2-HYDROXYQUINOLINE

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:2217-31-4 SDS

2217-31-4Relevant articles and documents

Synthesis of 3-alkyl-1H-quinolin-2-ones via palladium-catalyzed intramolecular cyclization of benzyl halides and α,β-unsaturated amides

Liu, Zhangqin,Shi, Changqing,Chen, Yuanwei

experimental part, p. 1734 - 1736 (2009/04/10)

An efficient synthesis of 3-alkyl-1H-quinolin-2-ones was achieved in high yield (up to 91%) via Pd2(dba)3-catalyzed intramolecular cyclization of benzyl halides and electron-deficient olefins, followed by treatment with DBU. Thieme S

Transformation of Quinazoline into 2(1H)-Quinolinones with Alkanoic Anhydrides

Higashino, Takeo,Goto, Ayako,Miyashita, Akira,Hayashi, Eisaku

, p. 4352 - 4355 (2007/10/02)

Quinazoline (1) was transformed into 3-substituted 2(1H)-quinolinones (4) by reaction with alkanoic anhydrides (3).Similar transformation was also found to occur with 5-methyl-1-phenyl-1H-pyrazolopyrimidinium iodide (9), giving 5-substituted 1-phenyl-1H-pyrazolo-pyridine-6-yl alkanoates (10).Keywords-quinazoline; quinolinone; alkanoic anhydride; ring transformation; pyrazolo-pyrimidinium salt; pyrazolopyridine

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