64254-02-0 Usage
Derivative of indole
Heterocyclic aromatic organic compound This compound is derived from indole, which is a heterocyclic aromatic organic compound. This means that it contains a ring structure with atoms such as carbon and nitrogen, and it has a characteristic aromatic smell.
Building block in synthesis
Pharmaceuticals and agrochemicals 1H-Indole-2-carbonitrile, 1,3-dimethylis commonly used as a building block in the synthesis of various pharmaceuticals and agrochemicals. This means that it is a key component in the creation of these products and is used in the development of new drugs.
Application
Medicines, dyes, and organic chemicals The compound has a wide range of applications, including the production of medicines, dyes, and organic chemicals. This indicates that it is an important substance in various industries.
Biological activities
Potential use in pharmaceutical industry 1H-Indole-2-carbonitrile, 1,3-dimethylis known for its potential biological activities, which means that it may have effects on living organisms. This makes it a valuable substance in the pharmaceutical industry for the development of new drugs.
Use in research
Organic synthesis Additionally, 1H-Indole-2-carbonitrile, 1,3-dimethylis used in research laboratories for chemical reactions and studies related to organic synthesis. This means that it is an important substance for understanding and developing new organic compounds.
Check Digit Verification of cas no
The CAS Registry Mumber 64254-02-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,4,2,5 and 4 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 64254-02:
(7*6)+(6*4)+(5*2)+(4*5)+(3*4)+(2*0)+(1*2)=110
110 % 10 = 0
So 64254-02-0 is a valid CAS Registry Number.
64254-02-0Relevant articles and documents
Site-Selective Electrochemical C-H Cyanation of Indoles
Li, Laiqiang,Hou, Zhong-Wei,Li, Pinhua,Wang, Lei
supporting information, p. 5983 - 5987 (2021/08/16)
An electrochemical approach for the site-selective C-H cyanation of indoles employing readily available TMSCN as cyano source has been developed. The electrosynthesis relies on the tris(4-bromophenyl)amine as a redox catalyst, which achieves better yield and regioselectivity. A variety of C2- and C3-cyanated indoles were obtained in satisfactory yields. The reactions are conducted in a simple undivided cell at room temperature and obviate the need for transition-metal reagent and chemical oxidant.
