623177-14-0 Usage
Description
7-CHLORO-2-METHYL-1H-INDOLE, also known as 2-Chloro-7-methylindole, is a chemical compound that belongs to the indole class of organic compounds. It is a halogenated derivative of indole, characterized by the presence of a chlorine atom at the 7 position and a methyl group at the 2 position of the indole ring. This yellow solid is soluble in organic solvents, has a distinctive odor, and should be handled with caution due to its potential harmful effects if ingested or inhaled.
Uses
Used in Pharmaceutical Industry:
7-CHLORO-2-METHYL-1H-INDOLE is used as a building block in the synthesis of pharmaceuticals for its versatile chemical properties, contributing to the development of new drugs and therapeutic agents.
Used in Chemical Research:
7-CHLORO-2-METHYL-1H-INDOLE serves as a research tool in the study of indole-based compounds, aiding scientists in understanding their biological activities and potential applications in various fields.
Used in Organic Chemistry:
7-CHLORO-2-METHYL-1H-INDOLE is utilized in organic chemistry for its reactivity and structural features, enabling the synthesis of a wide range of organic molecules with diverse applications.
Check Digit Verification of cas no
The CAS Registry Mumber 623177-14-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,2,3,1,7 and 7 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 623177-14:
(8*6)+(7*2)+(6*3)+(5*1)+(4*7)+(3*7)+(2*1)+(1*4)=140
140 % 10 = 0
So 623177-14-0 is a valid CAS Registry Number.
623177-14-0Relevant articles and documents
Synthesis of Indoles by Palladium-Catalyzed Reductive Cyclization of β-Nitrostyrenes with Carbon Monoxide as the Reductant
Ferretti, Francesco,El-Atawy, Mohamed A.,Muto, Stefania,Hagar, Mohamed,Gallo, Emma,Ragaini, Fabio
, p. 5712 - 5715 (2015)
An efficient catalytic cyclization of β-nitrostyrenes to indoles was developed. The reaction was applied to the synthesis of 3-arylindoles and 2-alkylindoles. Given that in the latter case the starting β-nitrostyrenes can be easily obtained by a Henry reaction, the present method allows indoles to be obtained in a two-step sequence starting from cheap reactants.
