36193-65-4 Usage
General Description
1H-indole-2-carbonitrile is a chemical compound with the molecular formula C9H6N2. It belongs to the class of indole derivatives and is commonly used in organic synthesis and medicinal chemistry. It is a white to off-white solid with a melting point of 123-125°C. 1H-indole-2-carbonitrile is a versatile building block in the production of pharmaceuticals, agrochemicals, and dyes. It is known for its potential biological activities, including anti-cancer, anti-inflammatory, and antimicrobial properties. Its unique structure and reactivity make it a valuable intermediate in the synthesis of various compounds with diverse applications.
Check Digit Verification of cas no
The CAS Registry Mumber 36193-65-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,6,1,9 and 3 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 36193-65:
(7*3)+(6*6)+(5*1)+(4*9)+(3*3)+(2*6)+(1*5)=124
124 % 10 = 4
So 36193-65-4 is a valid CAS Registry Number.
36193-65-4Relevant articles and documents
Palladium-catalyzed synthesis of 2-cyanoindoles from 2-gem-dihalovinylanilines
Zeidan, Nicolas,Bognar, Sabine,Lee, Sophia,Lautens, Mark
supporting information, p. 5058 - 5061 (2017/11/07)
An efficient Pd(0)-catalyzed synthesis of 2-cyanoindoles from 2-gem-dihalovinylanilines is reported. Few methods have aimed to synthesize these scaffolds which are found in many natural products and have high bioactivity. This protocol features a robust c
2-(Tosylamino)benzyltrimethylammonium halides as precursors of 2-substituted indoles
Croce, Piero Dalla,Ferraccioli, Raffaella,La Rosa, Concetta
, p. 2397 - 2407 (2007/10/03)
The reactions of 2-(tosylamino)benzyltrimethylammonium halides (1) with dimethylsulfonium 2-oxo-2-phenylethylide (6b), dimethylsulfonium 2-ethoxy-2-oxo-ethylide (6c) and dimethylsulfonium cyanomethylide (6d) are useful synthetic routes to 2-substituted indoles (8b-d). The relationship between reaction conditions and selectivity is discussed.
