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6-tert-Butyl-quinolin-4-ol is a chemical compound characterized by a quinoline ring with a tertiary butyl group and a hydroxy group attached to it. It is recognized for its strong chelating properties, which enable it to form stable complexes with metal ions, and its potential as an antioxidant and radical scavenger. This versatile compound is utilized in various industrial and commercial applications, including the synthesis of pharmaceuticals, production of synthetic dyes, pigments, and polymers, and has shown promise in medicinal chemistry due to its ability to inhibit certain enzymes and receptors.

444609-92-1

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444609-92-1 Usage

Uses

Used in Pharmaceutical Industry:
6-tert-Butyl-quinolin-4-ol is used as an intermediate in the synthesis of various pharmaceuticals for its ability to form stable complexes with metal ions, which can enhance the efficacy and stability of the final drug products.
Used as an Antioxidant and Radical Scavenger:
In different industrial and commercial applications, 6-tert-Butyl-quinolin-4-ol is used as an antioxidant and radical scavenger to protect materials from oxidative damage and extend their shelf life.
Used in the Production of Synthetic Dyes, Pigments, and Polymers:
6-tert-Butyl-quinolin-4-ol is utilized in the production of synthetic dyes, pigments, and polymers due to its chemical properties that contribute to the color, stability, and performance of these materials.
Used in Medicinal Chemistry:
6-tert-Butyl-quinolin-4-ol is used in the field of medicinal chemistry for its potential to inhibit certain enzymes and receptors, which can lead to the development of new drugs with therapeutic benefits.

Check Digit Verification of cas no

The CAS Registry Mumber 444609-92-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,4,4,6,0 and 9 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 444609-92:
(8*4)+(7*4)+(6*4)+(5*6)+(4*0)+(3*9)+(2*9)+(1*2)=161
161 % 10 = 1
So 444609-92-1 is a valid CAS Registry Number.
InChI:InChI=1/C13H15NO/c1-13(2,3)9-4-5-11-10(8-9)12(15)6-7-14-11/h4-8H,1-3H3,(H,14,15)

444609-92-1Relevant academic research and scientific papers

Synthesis of novel halogenated 4(1H)-quinolones by thermolysis of arylaminomethylene-1,3-dioxane-4,6-diones

Rotzoll, Sven,Reinke, Helmut,Fischer, Christine,Langer, Peter

experimental part, p. 69 - 78 (2009/06/17)

A variety of novel 4(1H)-quinolone derivatives were prepared by thermolysis of aminomethylene Meldrum's acid derivatives. Georg Thieme Verlag Stuttgart.

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