13228-40-5 Usage
Uses
Used in Pharmaceutical Industry:
2-PYRIDIN-2-YL-1H-INDOLE is used as a key intermediate in the synthesis of pharmaceuticals for its ability to be incorporated into various drug molecules, enhancing their therapeutic properties.
Used in Agrochemical Industry:
In agrochemicals, 2-PYRIDIN-2-YL-1H-INDOLE is utilized as a building block for the development of novel compounds with pesticidal or herbicidal activities, contributing to more effective crop protection strategies.
Used in Medicinal Chemistry:
2-PYRIDIN-2-YL-1H-INDOLE is employed as a molecular scaffold in medicinal chemistry for the design and synthesis of new bioactive molecules with potential applications in treating various diseases.
Used in Material Science:
2-PYRIDIN-2-YL-1H-INDOLE is also used as a component in the development of advanced materials, leveraging its unique structural and electronic properties.
Used in Anticancer Research:
2-PYRIDIN-2-YL-1H-INDOLE is studied as a potential anticancer agent, showing promise in inhibiting the growth of cancer cells, thus contributing to the discovery of new cancer therapeutics.
Used in Organic Synthesis:
As a versatile organic compound, 2-PYRIDIN-2-YL-1H-INDOLE is used as a reagent or building block in organic synthesis for creating a wide range of organic compounds with diverse applications.
Check Digit Verification of cas no
The CAS Registry Mumber 13228-40-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,2,2 and 8 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 13228-40:
(7*1)+(6*3)+(5*2)+(4*2)+(3*8)+(2*4)+(1*0)=75
75 % 10 = 5
So 13228-40-5 is a valid CAS Registry Number.
InChI:InChI=1/C13H10N2/c1-2-6-11-10(5-1)9-13(15-11)12-7-3-4-8-14-12/h1-9,15H
13228-40-5Relevant academic research and scientific papers
Photo-Arylation. VII. Photoreaction of 2-Halopyridine with Indole
Seki, Koh-Ichi,Ohkura, Kazuke,Terashima, Masanao,Kanaoka, Yuichi
, p. 940 - 944 (2007/10/02)
Photolysis of 2-halopyridine with indole afforded the (2-pyridyl)indoles as a regioisomeric mixture.On the basis of the isomer distributions, an electron transfer mechanism is suggested for the present reaction.The regioselectivity was found to be fairly dependent on the solvent polarity. Keywords---(2-pyridyl)indole; photoarylation; photolysis; 2-halopyridine; indole; electron transfer; solvent effect; isomer distribution
Deoxygenation Reactions of ortho-Nitrostyrenes with Carbon Monoxide Catalysed by Metal Carbonyls: a New Route to Indoles
Crotti, Corrado,Cenini, Sergio,Rindone, Bruno,Tollari, Stefano,Demartin, Francesco
, p. 784 - 786 (2007/10/02)
The metal carbonyls Fe(CO)5, Ru3(CO)12, and Rh6(CO)16 are catalysts for the deoxygenation of ortho-nitrostyrenes under carbon monoxide pressure to give indole derivatives; the crystal structure of a non-catalytically active rhodium complex obtained during the synthesis of (5e) is reported.
