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3-Methoxyquinoline, a derivative of quinoline with the molecular formula C10H9NO, is a yellowish-brown solid characterized by a distinct odor. It is soluble in organic solvents and has been recognized for its potential biological and pharmacological activities, such as antioxidant and anti-inflammatory properties. This chemical compound plays a significant role in the pharmaceutical industry, primarily as an intermediate or building block for the synthesis of various pharmaceutical drugs and organic compounds.

6931-17-5

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6931-17-5 Usage

Uses

Used in Pharmaceutical Industry:
3-Methoxyquinoline is used as a chemical intermediate for the synthesis of various pharmaceutical drugs and organic compounds. Its unique structure and properties make it a valuable component in the development of new medications and therapeutic agents.
Used in Research and Development:
3-Methoxyquinoline is utilized as a research compound to study its potential biological and pharmacological activities. Its antioxidant and anti-inflammatory properties are of particular interest, as they may contribute to the development of novel treatments for various diseases and conditions.
Used in Organic Synthesis:
As a versatile chemical compound, 3-Methoxyquinoline is employed in organic synthesis for the preparation of a wide range of organic compounds. Its reactivity and functional groups make it a suitable candidate for various chemical reactions, leading to the formation of new molecules with potential applications in various industries.

Check Digit Verification of cas no

The CAS Registry Mumber 6931-17-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,9,3 and 1 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 6931-17:
(6*6)+(5*9)+(4*3)+(3*1)+(2*1)+(1*7)=105
105 % 10 = 5
So 6931-17-5 is a valid CAS Registry Number.

6931-17-5Relevant academic research and scientific papers

Photochemistry of Methoxy-substituted Quinoline and Isoquinoline N-Oxides

Albini, Angelo,Fasani, Elisa,Dacrema, Lucia Maggi

, p. 2738 - 2742 (2007/10/02)

The photochemistry of quinoline 1-oxides and isoquinoline 2-oxides bearing a methoxy-group in the pyridine ring was investigated in protic and aprotic media.The formation of various photoisomers, viz. 3,1-benzoxazepines, 2(1H)-quinolones, N-(2-isocyanobenzyl)formamides, 4(1H)-quinolones, and 3-hydroxyquinolines from the different methoxyquinoline 1-oxides, and 1,3-benzoxazepines and 1(2H)-isoquinolones from the different methoxyisoquinoline 2-oxides, was observed along with deoxygenation and formation of products derived from hydration and decomposition of the primary products.The position of the methoxy-group has an important directing effect on the photoreactions.

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