6632-15-1

Usage

Uses

Used in Agricultural Industry:
2,4-dichloro-N-(prop-2-en-1-yl)aniline is used as a herbicide and pesticide for controlling and eliminating unwanted vegetation and pests. It helps protect crops from damage caused by weeds and other unwanted plants, ensuring a healthy and productive agricultural yield.
As a Herbicide:
2,4-dichloro-N-(prop-2-en-1-yl)aniline is used as a herbicide to control the growth of unwanted plants and weeds in agricultural fields. It targets specific plant species, allowing farmers to maintain a clean and productive crop environment.
As a Pesticide:
2,4-dichloro-N-(prop-2-en-1-yl)aniline is also used as a pesticide to protect crops from pests and insects that can cause significant damage to the plants. By controlling these pests, it helps maintain the health and quality of the crops.
However, it is important to note that 2,4-dichloro-N-(prop-2-en-1-yl)aniline is considered to be moderately toxic to humans and the environment. Therefore, proper precautions should be taken when handling and using this chemical to minimize potential risks and ensure the safety of both people and the environment.

Upstream product

• 589-09-3 N-allyl-N-phenylamine 
• 554-00-7 2,4-Dichloroaniline 
• 106-95-6 allyl bromide 

Downstream Products

• 1255773-53-5 2-allyl-4,6-dichloroaniline 

Relevant academic research and scientific papers

Taming chlorine azide: Access to 1,2-azidochlorides from alkenes

The in situ preparation and trapping of chlorine azide provided a versatile one-pot method for the azidochlorination of alkenes. Gaseous ClN3 generated from sodium azide, hypochlorite, and acetic acid can be explosive if isolation is attempted. Instead, we generated the reagent in biphasic media in the presence of olefinic compounds dissolved in the organic layer or evenly emulsified throughout the solution in the absence of organic solvent. Under these conditions, ClN3 is created slowly and trapped immediately at the aqueous-organic interface. The resulting safe and reliable procedure provided 1,2-azidochloride derivatives of a variety of substrates, with evidence for both polar and radical mechanisms. Minor impurities characterized in the product mixtures indicated the presence of alternative reaction pathways deriving primarily from radical intermediates.

Efficient copper-catalyzed direct intramolecular aminotrifluoromethylation of unactivated alkenes with diverse nitrogen-based nucleophiles

A mild, convenient, and step-economical intramolecular aminotrifluoromethylation of unactivated alkenes with a variety of electronically distinct, nitrogen-based nucleophiles in the presence of a simple copper salt catalyst, in the absence of extra ligand