6851-40-7

Basic information

• Product Name: 2,4-dichloro-1-isopropoxybenzene
• Synonyms: 2,4-dichloro-1-isopropoxybenzene
• CAS NO: 6851-40-7
• Molecular Formula: C₉H₁₀Cl₂O
• Molecular Weight: 205.0811
• Mol File: 6851-40-7.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 250.5±20.0 °C(Predicted)
• Appearance: /
• Density: 1.201±0.06 g/cm3(Predicted)
• CAS DataBase Reference: 2,4-dichloro-1-isopropoxybenzene(CAS DataBase Reference)
• NIST Chemistry Reference: 2,4-dichloro-1-isopropoxybenzene(6851-40-7)
• EPA Substance Registry System: 2,4-dichloro-1-isopropoxybenzene(6851-40-7)

Safety Data

• Hazardous Substances Data: 6851-40-7(Hazardous Substances Data)

Usage

General Description

2,4-dichloro-1-isopropoxybenzene, also known as 2,4-DIPB, is a chemical compound with the molecular formula C9H10Cl2O. It is an aromatic ether and a chlorinated derivative of phenol. 2,4-dichloro-1-isopropoxybenzene is used in the manufacturing of various products, including pesticides and herbicides. It is also used as an intermediate in the production of other chemicals. 2,4-DIPB has potential health hazards and should be handled with care. It is important to follow safety protocols and regulations when working with this chemical to avoid any adverse effects on human health and the environment.

Upstream product

• 1435-48-9 1,3-dichloro-4-fluorobenzene 
• 67-63-0 isopropyl alcohol 
• 75-26-3 isopropyl bromide 
• 120-83-2 2,4-dichlorophenol 
• 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 

Relevant articles and documents

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.

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.