6851-40-7

Usage

Uses

Used in Pesticide and Herbicide Manufacturing:
2,4-dichloro-1-isopropoxybenzene is used as a key intermediate in the synthesis of various pesticides and herbicides. Its chemical structure allows for the creation of active ingredients that can effectively control and eliminate unwanted plant and insect species.
Used in Chemical Production:
2,4-DIPB is also utilized as an intermediate in the production of other chemicals, contributing to the synthesis of a wide range of compounds with diverse applications in various industries.
Safety Considerations:
Due to its potential health hazards, 2,4-dichloro-1-isopropoxybenzene should be handled with care. It is crucial to follow safety protocols and regulations when working with this chemical to minimize the risk of adverse effects on human health and the environment.

Upstream product

• 1435-48-9 1,3-dichloro-4-fluorobenzene 
• 67-63-0 isopropyl alcohol 
• 19666-30-9 3-[2,4-dichloro-5-(1-methylethoxy)phenyl]-5-(1,1-dimethylethyl)-1,3,4-oxadiazol-2(3H)-one 
• 75-30-9 2-iodo-propane 
• 120-83-2 2,4-dichlorophenol 
• 75-26-3 isopropyl bromide 

Relevant academic research and scientific papers

Organophotochemical SNAr Reactions of Mildly Electron-Poor Fluoroarenes

C–F functionalization of arenes with a range of alcohol and pyrazole nucleophiles has been achieved without the need for metal catalysts or highly electron-poor substrates. Treatment of fluoroarenes with alcohols or pyrazoles and DDQ under irradiation by blue LED light provides the corresponding substituted products. The procedure is complementary to classical SNAr chemistry which generally requires basic reaction conditions and high temperatures, and provides products under non-basic conditions at ≈ 40 °C.

Optimization of 5-(2,6-dichlorophenyl)-3-hydroxy-2-mercaptocyclohex-2-enones as potent inhibitors of human lactate dehydrogenase

Optimization of 5-(2,6-dichlorophenyl)-3-hydroxy-2-mercaptocyclohex-2-enone using structure-based design strategies resulted in inhibitors with considerable improvement in biochemical potency against human lactate dehydrogenase A (LDHA). These potent inhi

Microbial Degradation of Oxadiazon by Soil Fungus Fusarium solani

Degradation of oxadiazon 2-1,3,4-oxadiazolin-5-one (1)>, a preemergent soil-applied herbicide, by a soil fungus, Fusarium solani (Mortius) Sacc., has been investigated.F. solani, isolated from soil by enrichment culture technique, degraded the herbicide 1 by cometabolic process.Eleven metabolites have been isolated, out of which three metabolites (M1, M2, and M3) were characterized by spectroscopic evidence.Metabolites M1 and M3 are reported for the first time as metabolites of oxadiazon.The main metabolic pathways involve oxadiazoline ring cleavage without dechlorination reaction. - Keywords: degradation; cometabolism; metabolic pathway; oxadiazon; Fusarium solani.