Persistence and transformation of the herbicides [14C]fenoxaprop-ethyl and [14C]fenthiaprop-ethyl in two prairie soils under laboratory and field conditions was written by Smith, Allan E.. And the article was included in Journal of Agricultural and Food Chemistry in 1985.Application In Synthesis of 6-Chlorobenzo[d]thiazol-2(3H)-one This article mentions the following:
The exptl. herbicidal esters fenoxaprop-ethyl (I) [66441-23-4] and fenthiaprop-ethyl (II) [95617-09-7] both underwent almost complete hydrolysis within 24 h to their resp. acids in soils with moisture contents >65% of field capacity. In air-dried soils, ester hydrolysis was considerably less. The fate of the 2 14C-labeled esters was studied in 2 soil types under laboratory and field conditions. Each herbicide gave rise to the same transformation products in the laboratory and field studies. Fenthiaprop acid [73519-50-3] and its corresponding transformation products, i.e., a phenetole [95617-11-1], phenol [70216-88-5], and a benzthiazolone [62266-81-3], have a soil persistence of about twice that of fenoxaprop acid and corresponding transformation products. In the experiment, the researchers used many compounds, for example, 6-Chlorobenzo[d]thiazol-2(3H)-one (cas: 62266-81-3Application In Synthesis of 6-Chlorobenzo[d]thiazol-2(3H)-one).
6-Chlorobenzo[d]thiazol-2(3H)-one (cas: 62266-81-3) belongs to thiazole derivatives. Thiazoles in peptides or their ability to bind proteins, DNA and RNA has led to many synthetic studies and new applications. Thiazole is a versatile building block for the construction and lead generation of new drug discoveries. Numerous diazole-based compounds are in clinical use as anticancer, antileukemic, antiinflammatory, antiviral, antifungal, antirheumatic, immunomodulator, and antiparasitic agents.Application In Synthesis of 6-Chlorobenzo[d]thiazol-2(3H)-one
Referemce:
Thiazole | C3H3NS – PubChem,
Thiazole | chemical compound | Britannica