877264-48-7

Usage

Uses

Used in Pharmaceutical Industry:
Benzo[b]thiophen-6-yl trifluoromethanesulfonate is used as a reagent for the synthesis of various pharmaceuticals, contributing to the development of new drugs and therapeutic agents. Its role in organic synthesis allows for the creation of complex molecules that can be utilized in medicinal chemistry.
Used in Agrochemical Industry:
In the agrochemical sector, Benzo[b]thiophen-6-yl trifluoromethanesulfonate is employed as a reagent in the synthesis of agrochemicals, such as pesticides and herbicides. Its application in this industry aids in the development of effective and innovative products for agricultural use.
Used in Organic Synthesis:
Benzo[b]thiophen-6-yl trifluoromethanesulfonate is used as a nucleophile in organic chemistry reactions, enabling the formation of new chemical bonds and the synthesis of complex organic molecules. Its versatility in this role makes it a valuable component in the field of organic synthesis.

Upstream product

• 19301-39-4 1-benzothiophen-6-ol 
• 358-23-6 trifluoromethylsulfonic anhydride 

Downstream Products

• 29813-41-0 6-acetylbenzothiophene 

Relevant academic research and scientific papers

Aryl- and heteroaryl-substituted tetrahydroisoquinolines and use thereof to block reuptake of norepinephrine, dopamine, and serotonin

The compounds of the present invention are represented by the chemical structure found in Formula (I): wherein: the carbon atom designated * is in the R or S configuration; and X is a fused bicyclic carbocycle or heterocycle selected from the group consisting of benzofuranyl, benzo[b]thiophenyl, benzoisothiazolyl, benzoisoxazolyl, indazolyl, indolyl, isoindolyl, indolizinyl, benzoimidazolyl, benzooxazolyl, benzothiazolyl, benzotriazolyl, imidazo[1,2-a]pyridinyl, pyrazolo[1,5-a]pyridinyl, [1,2,4]triazolo[4,3-a]pyridinyl, thieno[2,3-b]pyridinyl, thieno[3,2-b]pyridinyl, 1H-pyrrolo[2,3-b]pyridinyl, indenyl, indanyl, dihydrobenzocycloheptenyl, tetrahydrobenzocycloheptenyl, dihydrobenzothiophenyl, dihydrobenzofuranyl, indolinyl, naphthyl, tetrahydronaphthyl, quinolinyl, isoquinolinyl, 4H-quinolizinyl, 9aH-quinolizinyl, quinazolinyl, cinnolinyl, phthalazinyl, quinoxalinyl, benzo[1,2,3]triazinyl, benzo[1,2,4]triazinyl, 2H-chromenyl, 4H-chromenyl, and a fused bicyclic carbocycle or fused bicyclic heterocycle optionally substituted with substituents (1 to 4 in number) as defined in R14; with R1, R2, R3, R4, R5, R6, R7, R8, and R14 defined herein.