86763-47-5

Basic information

• Product Name: Propisochlor
• Synonyms: 2-Chloro-N-(2-ethyl-6-methylphenyl)-N-(isopropoxymethyl)acetamide;2-CHLORO-2'-ETHYL-6'-METHYL-N-(ISOPROPOXYMETHYL)ACETANILIDE;PROPONIT;PROPISOCHLOR;propisochlor (bsii,pa e-iso);propisochlore ((m) pa f-iso);Proponit, 2-Chloro-2μ-ethyl-6μ-methyl-N-(isopropoxymethyl)acetanilide;Propisochlor 5
• CAS NO: 86763-47-5
• Molecular Formula: C₁₅H₂₂ClNO₂
• Molecular Weight: 283.79
• Mol File: 86763-47-5.mol
• Article Data: 2

Chemical Properties

• Melting Point: 21.6 °C
• Boiling Point: 399.3 °C at 760 mmHg
• Flash Point: 195.3 °C
• Appearance: white-off solid or colorless liquid
• Density: 1.1 g/cm³
• Vapor Pressure: 1.38E-06mmHg at 25°C
• Refractive Index: 1.533
• Storage Temp.: 2-8°C
• Solubility: Chloroform, Ethyl Acetate (Slightly)
• PKA: 1.30±0.50(Predicted)
• CAS DataBase Reference: Propisochlor(CAS DataBase Reference)
• NIST Chemistry Reference: Propisochlor(86763-47-5)
• EPA Substance Registry System: Propisochlor(86763-47-5)

Safety Data

• Hazard Codes: Xn
• Statements: 21
• Safety Statements: 36/37
• WGK Germany: 3
• Hazardous Substances Data: 86763-47-5(Hazardous Substances Data)

Usage

Uses

Propisochlor is an herbicide that is absorbed through the shoots of germinating plants.

InChI:InChI=1/C15H22ClNO2/c1-5-13-8-6-7-12(4)15(13)17(14(18)9-16)10-19-11(2)3/h6-8,11H,5,9-10H2,1-4H3

Upstream product

• 24549-06-2 6-ethyl-o-toluidine 
• 79-04-9 chloroacetyl chloride 

Relevant articles and documents

Synthesizing method for chloroacetamide compound

The invention discloses a synthesizing method for a chloroacetamide compound. In a reaction kettle, a secondary amine compound is dissolved in an organic solvent, the mixture is heated for reflux, chloroacetyl chloride is added into the mixture, a reflux reaction is conducted for 0.5-20 hours, and the chloroacetamide compound is obtained. According to the synthesizing method for the chloroacetamide compound, an acid binding agent is not used, discharging of wastewater in the after-treatment process is reduced, by keeping the reflux state of the system, hydrogen chloride gas generated from thereaction is exhausted out of the system and absorbed by water outside the system, high-purity hydrochloric acid is obtained, the waste is turned into wealth, the method comes up to the production standard of safety and environment protection, and discharging of waste gas, waste water and waste residues is reduced; according to the synthesizing method for the chloroacetamide compound, few operationsteps are utilized, the reaction speed is high, the product yield is high, the purity is high, the production cost is low, and the method is safe, friendly to the environment and suitable for industrial large-scale production.