Enzyme inhibitors cause a decrease in the reaction rate of an enzyme-catalyzed reaction by binding to a specific portion of an enzyme and thus slowing or preventing a reaction from occurring. Safety of 3-(Bromomethyl)benzo[b]thiophene, C9H7BrS. A document type is Article, introducing its new discovery., Safety of 3-(Bromomethyl)benzo[b]thiophene
Easy access to fused tricyclic pyrrolo[1,2-a][1]benzothieno[2,3-e][1,4]diazepines from the corresponding carbonyl azides by thermolysis in acetic acid is described. Moreover, new [1]benzothieno[2,3(3,2)-f]indolizines were synthesized in one-pot from 2(3)-(2-formylpyrrol-1-ylmethyl)-[1]benzothiophene and with diethyl acetylenedicarboxylate (DEAD) they led regiospecifically to [3,2,2] cyclazines fused to a [1]benzothiophene ring by 1,3-dipolar cycloaddition reaction rather than Diels-Alder adducts.
The result showed that such a combination of chemo- and biocatalysis improved the catalytic yield more than two times compared with that of sole metal catalysis.I hope my blog about 1196-19-6 is helpful to your research.
Reference：
Benzothiophene – Wikipedia,
Benzothiophene | C8H6S – PubChem