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1(2H)-Acenaphthylenone, 2-(2-nitrophenyl)is a chemical compound characterized by the molecular formula C16H11NO3. It features an acenaphthylene backbone with a 2-(2-nitrophenyl) group attached, presenting a yellow solid appearance. 1(2H)-Acenaphthylenone, 2-(2-nitrophenyl)is insoluble in water but soluble in organic solvents, and it exhibits fluorescent properties, which makes it a versatile compound with potential applications in various fields.

189697-27-6

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189697-27-6 Usage

Uses

Used in Organic Synthesis:
1(2H)-Acenaphthylenone, 2-(2-nitrophenyl)is utilized as a building block in organic synthesis, contributing to the creation of more complex molecules and compounds. Its unique structure allows for a wide range of chemical reactions and modifications, making it a valuable component in the synthesis of various organic compounds.
Used in Fluorescence Spectroscopy and Imaging:
Due to its fluorescent properties, 1(2H)-Acenaphthylenone, 2-(2-nitrophenyl)is employed in the field of fluorescence spectroscopy and imaging. It serves as a marker or indicator in various analytical and diagnostic processes, providing valuable information about molecular interactions, structural changes, and other phenomena at the molecular level.
Used in Chemical Reactions as a Reagent:
1(2H)-Acenaphthylenone, 2-(2-nitrophenyl)is also used as a reagent in different chemical reactions, where its specific properties can be harnessed to achieve desired outcomes. Its role as a reagent is crucial in the synthesis of various compounds and materials.
Used in Pharmaceutical Research:
1(2H)-Acenaphthylenone, 2-(2-nitrophenyl)has been studied for its potential biological activities and pharmacological applications. Its unique structure and properties make it a promising candidate for the development of new drugs and therapies, particularly in the areas of medicinal chemistry and drug discovery.
Used in the Chemical Industry:
In the chemical industry, 1(2H)-Acenaphthylenone, 2-(2-nitrophenyl)is used for the production of various specialty chemicals, dyes, and pigments. Its versatility in organic synthesis and its fluorescent properties make it a valuable component in the development of new products and materials with specific applications.

Check Digit Verification of cas no

The CAS Registry Mumber 189697-27-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,9,6,9 and 7 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 189697-27:
(8*1)+(7*8)+(6*9)+(5*6)+(4*9)+(3*7)+(2*2)+(1*7)=216
216 % 10 = 6
So 189697-27-6 is a valid CAS Registry Number.

189697-27-6Relevant academic research and scientific papers

Synthesis of 1-hydroxyindoles and indoles from ortho-nitroarylethanes

Wrobel, Zbigniew,Makosza, Mieczyslaw

, p. 5501 - 5514 (2007/10/03)

Cyclization of substituted ortho-nitroarylethanes to 1-hydroxyindoles and their further reduction to indoles is described. The mechanism of cyclization is discussed.

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