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1H-Indole, 1-acetyl-2-(2-naphthalenyl)-3-(phenylseleno)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

143879-58-7

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143879-58-7 Usage

Molecular Structure

A complex structure that includes an indole ring, acetyl group, naphthalene ring, and phenylseleno group.

Chemical Applications

Used in various chemical and pharmaceutical applications, such as a building block for the synthesis of biologically active compounds.

Potential Applications

Possibility for development of new drugs and materials due to its unique structure and properties.

Structural Diversity

Provides opportunities for modification and optimization for specific applications.

Handling and Synthesis

Requires careful handling and synthesis procedures to ensure safety and purity in its use, due to its complex structure.

Check Digit Verification of cas no

The CAS Registry Mumber 143879-58-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,3,8,7 and 9 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 143879-58:
(8*1)+(7*4)+(6*3)+(5*8)+(4*7)+(3*9)+(2*5)+(1*8)=167
167 % 10 = 7
So 143879-58-7 is a valid CAS Registry Number.

143879-58-7Downstream Products

143879-58-7Relevant academic research and scientific papers

Synthesis of Indoles via Amidoselenation

Izumi, Taeko,Sugano, Miwa,Konno, Touru

, p. 899 - 904 (2007/10/02)

The reaction of 2-styrylacetanilides (2) with N-phenylselenosuccinimide affords 1-N-acetyl-2-phenyl-3-phenylselenoindoles (3) and 1-N-acetyl-2-phenylindoles (4).The reaction of 2-vinylacetanilides (5) with phenylselenenyl bromide proceeds to form indoles via an intramolecular amidoselenation.

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