2217-31-4 Usage
Uses
Used in Pharmaceutical Industry:
3-Ethyl-2-hydroxyquinoline is used as a pharmaceutical agent for its potential antifungal, antibacterial, and antioxidant activities. Its pharmacological properties make it a promising candidate for the development of new drugs and therapies.
Used in Agricultural Industry:
3-Ethyl-2-hydroxyquinoline is used as an agricultural chemical for its potential applications in crop protection and enhancement of crop yield. Its antifungal and antibacterial properties can help in controlling plant diseases and promoting healthy growth.
Used in Material Development:
3-Ethyl-2-hydroxyquinoline is used in the development of new materials due to its unique chemical structure and properties. It can be utilized in the creation of advanced materials for various applications, including electronics, coatings, and composites.
Used as a Chelating Agent in Chemical Processes:
3-Ethyl-2-hydroxyquinoline is used as a chelating agent in chemical processes to bind and stabilize metal ions. This property can be useful in various industrial applications, such as water treatment, catalysis, and the synthesis of metal-organic frameworks.
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)
2217-31-4Relevant academic research and scientific papers
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
Electrophilic Substitution in 3- and 4-Methyl-2(1H)quinolinone through Metallated Species
Martin, Olga,Cuesta de la, Elena,Avendano, Carmen
, p. 7547 - 7554 (2007/10/02)
Unprotected 3- (2) and 4-methyl-2(1H)quinolinones (3a) and 4-methyl-5,8-dimethoxy-2(1H)quinolinone (3b) undergo through regioselective lithiation chain enlargement with different electrophiles.
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
