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1H-Indole, 3-ethyl-2-propyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

17901-63-2

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17901-63-2 Usage

Chemical Class

Indole class of organic compounds

Structure

Bicyclic structure containing a benzene ring fused to a pyrrole ring

Substitution

Substituted indole with an ethyl group at position 3 and a propyl group at position 2 of the indole ring

Usage

Commonly used in the synthesis of pharmaceuticals, agrochemicals, and other organic compounds

Biological Activities

Exhibits a variety of biological activities, including anti-inflammatory, antimicrobial, and anticancer properties

Importance

Valuable building block for the development of novel drugs and chemical substances

Check Digit Verification of cas no

The CAS Registry Mumber 17901-63-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,9,0 and 1 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 17901-63:
(7*1)+(6*7)+(5*9)+(4*0)+(3*1)+(2*6)+(1*3)=112
112 % 10 = 2
So 17901-63-2 is a valid CAS Registry Number.

17901-63-2Downstream Products

17901-63-2Relevant academic research and scientific papers

Fischer indole synthesis in the absence of a solvent

Matsumoto, Kiyoshi,Tanaka, Akinori,Yukio, Ikemi,Hayashi, Naoto,Toda, Mitsuo,Bulman, Robert A.

, p. 9 - 12 (2007/10/03)

The traditional Fischer synthesis of indoles has been investigated and it has been shown that the reaction proceeds in good yield in the absence of a solvent.

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