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2-Benzoyl-1H-indole-3-carbonitrile is an organic compound with the molecular formula C15H8N2O. It is a derivative of indole, a heterocyclic aromatic organic compound, and features a benzoyl group (a benzene ring with a carbonyl group) attached to the 2-position of the indole ring and a nitrile group (C≡N) at the 3-position. 2-Benzoyl-1H-indole-3-carbonitrile is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals due to its unique chemical structure. It is typically synthesized through chemical reactions involving indole and benzoyl chloride, and its properties, such as solubility and reactivity, can be influenced by the presence of substituents on the indole ring. The compound is an important intermediate in the preparation of more complex molecules, particularly in the field of medicinal chemistry.

98508-87-3

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98508-87-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 98508-87-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,8,5,0 and 8 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 98508-87:
(7*9)+(6*8)+(5*5)+(4*0)+(3*8)+(2*8)+(1*7)=183
183 % 10 = 3
So 98508-87-3 is a valid CAS Registry Number.

98508-87-3Downstream Products

98508-87-3Relevant academic research and scientific papers

One-pot syntheses of 3-cyanoindoles from 3-acyl- and 3-ethoxycarbonyl-1,2-dihydrocinnoline-1,2-dicarboximides

Tanaka, Satoko,Seguchi, Kazuyoshi,Sera, Akira

, p. 519 - 520 (1995)

2-Acyl- and 2-ethoxycarbonyl-3-cyanoindoles were prepared from 3-acyl- and 3-ethoxycarbonyl-1,2-dihydrocinnoline-1,2-dicarboximides and potassium cyanide via Michael addition, skeletal rearrangement and subsequent elimination of isocyanate.

A NOVEL SYNTHESIS OF 3-CYANOINDOLES AND A NEW ROUTE TO INDOLE-3-CARBOXYLIC ACID DERIVATIVES.

Garcia, Josefina,Greenhouse, Robert,Muchowski, Joseph M.,Ruiz, Jose Antonio

, p. 1827 - 1830 (2007/10/02)

2-Alkyl-3-cyanoindoles are obtained when 1-alkylmethyl-2-chloro-(or 2-phenylsulfonyl)-3-phenylsulfonylindoles are reacted with excess azide ion (90 deg C/DMF).The reaction is considered to occur by a fragmentation recombination process in which the Schiff

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