35582-11-7

Usage

Uses

Used in Agricultural and Horticultural Industries:
2-(3-Methoxyphenyl)ethanethioamide is used as a herbicide and plant growth regulator for controlling and managing the growth of unwanted grasses and weeds. It works by inhibiting the enzyme acetolactate synthase, which is essential for the biosynthesis of branched-chain amino acids in plants, leading to the inability of targeted plants to grow and eventually die off. This helps protect crops and turf from invasive and unwanted vegetation.
It is important to handle and apply 2-(3-Methoxyphenyl)ethanethioamide with care, as it is toxic to aquatic organisms and may have harmful effects on the environment if not used properly.

InChI:InChI=1/C9H11NOS/c1-11-8-4-2-3-7(5-8)6-9(10)12/h2-5H,6H2,1H3,(H2,10,12)

Upstream product

• 19924-43-7 3-methoxyphenylacetonitrile 

Downstream Products

• 250258-72-1 2-{2-[2-(3-methoxy-benzyl)-thiazol-4-yl]-ethyl}-isoindole-1,3-dione 
• 1318757-14-0 N-[2-(3-hydroxybenzyl)-4-methyl-1,3-thiazol-5-yl]-1-methyl-1H-pyrazole-5-carboxamide 
• 1318757-08-2 N-[2-(3-methoxybenzyl)-4-methyl-1,3-thiazol-5-yl]-1-methyl-1H-pyrazole-5-carboxamide 
• 1318758-23-4 tert-butyl [2-(3-methoxybenzyl)-4-methyl-1,3-thiazol-5-yl]carbamate 
• 1053656-78-2 2-(3-methoxybenzyl)-4-methyl-1,3-thiazole-5-carboxylic acid 
• 1318758-22-3 ethyl 2-(3-methoxybenzyl)-4-methyl-1,3-thiazole-5-carboxylate 

Relevant academic research and scientific papers

THIAZOLE DERIVATIVE

Provided is a compound having an agonist action on GPR52, which is useful as a prophylactic or therapeutic drug for mental diseases such as schizophrenia and the like, and the like. A compound represented by the formula (I): wherein each symbol is as defi

Phosphorus pentasulfide: A mild and versatile reagent for the preparation of thioamides from nitriles

A simple, efficient, and new method has been developed for the synthesis of thioamides from nitriles. The reaction of a variety of aromatic and aliphatic nitriles in the presence of phosphorus pentasulfide afforded the corresponding thioamides in high yields. This method is easy, rapid, and high-yielding for the synthesis of thioamides from nitriles. Georg Thieme Verlag Stuttgart.

Histamine H1 receptor ligands. Part I. Novel thiazol-4-ylethanamine derivatives: Synthesis and in vitro pharmacology

A series of 2-substituted thiazol-4-ylethanamines have been synthesized and tested for their histaminergic H1-receptor activities. The compounds with 2-phenyl substitution, regardless of the different physicochemical properties of the meta-substituents at the phenyl ring, showed weak H1-agonistic activity with pD2 values ranging from 4.35 to 5.36. When the phenyl group was replaced by a benzyl group, the resulting compounds all exhibited weak H1-antagonistic activity (pA2: 4.14-4.82). Copyright (C) 1999 Elsevier Science S.A.