885273-14-3 Usage
Description
5-(BENZOTHIOPHEN-2-YL)-1H-INDOLE is a chemical compound that belongs to the class of indole derivatives. It is comprised of a benzothiophene ring attached to the 5-position of the indole ring. 5-(BENZOTHIOPHEN-2-YL)-1H-INDOLE has potential use in the field of medicinal chemistry due to its diverse biological activities, including anticancer, anti-inflammatory, and antiviral properties. It may also have applications in the development of new pharmaceuticals and agrochemicals. Additionally, 5-(benzothiophen-2-yl)-1H-indole could serve as a valuable building block for the synthesis of more complex molecules in organic synthesis. Further research and exploration of its chemical and biological properties could lead to potential new therapeutic agents and other valuable applications.
Uses
Used in Pharmaceutical Industry:
5-(BENZOTHIOPHEN-2-YL)-1H-INDOLE is used as a potential therapeutic agent for its anticancer, anti-inflammatory, and antiviral properties. Its diverse biological activities make it a promising candidate for the development of new pharmaceuticals.
Used in Agrochemical Industry:
5-(BENZOTHIOPHEN-2-YL)-1H-INDOLE is used in the development of new agrochemicals, potentially offering novel solutions for pest control and crop protection.
Used in Organic Synthesis:
5-(BENZOTHIOPHEN-2-YL)-1H-INDOLE is used as a valuable building block for the synthesis of more complex molecules, contributing to the advancement of organic chemistry and the creation of new compounds with various applications.
Check Digit Verification of cas no
The CAS Registry Mumber 885273-14-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,8,5,2,7 and 3 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 885273-14:
(8*8)+(7*8)+(6*5)+(5*2)+(4*7)+(3*3)+(2*1)+(1*4)=203
203 % 10 = 3
So 885273-14-3 is a valid CAS Registry Number.
885273-14-3Relevant articles and documents
Flash generation of a highly reactive Pd catalyst for suzuki-miyaura coupling by using a flow microreactor
Nagaki, Aiichiro,Takabayashi, Naofumi,Moriwaki, Yuya,Yoshida, Jun-Ichi
, p. 11871 - 11875 (2012)
Superflash! Flash chemistry enables the use of highly reactive unstable species as catalysts for chemical synthesis. Fast micromixing of a solution of [Pd(OAc)2] and that of tBu3P in 1:1 mole ratio gave a solution of a highly reactive unstable species, which was immediately transferred to a vessel by using a flow microreactor, in which Suzuki-Miyaura coupling was conducted (see scheme). Copyright
