125488-14-4

Usage

Uses

Used in Agricultural Industry:
2,4-DICHLOROPHENACYL THIOCYANATE is used as a pesticide and insecticide for controlling a variety of pests that can damage crops. It is particularly effective on fruits, vegetables, and ornamental plants, where it helps protect these plants from infestations that could lead to reduced yields or compromised quality.
The application reason for using 2,4-DICHLOROPHENACYL THIOCYANATE in this context is its ability to inhibit the growth of insects and disrupt their hormonal balance, which ultimately results in the death of the pests. This action is crucial for maintaining the health and productivity of agricultural fields and gardens.
However, due to the toxic nature of 2,4-DICHLOROPHENACYL THIOCYANATE, it is imperative that it is handled with care and used strictly according to the recommended guidelines. This ensures the minimization of environmental and health risks associated with its use, balancing the benefits of effective pest control with the need for safety and sustainability.

InChI:InChI=1/C9H5Cl2NOS/c10-6-1-2-7(8(11)3-6)9(13)4-14-5-12/h1-3H,4H2

Upstream product

• 540-72-7 sodium thiocyanide 
• 2631-72-3 2,4-dichlorophenacyl bromide 
• 1147550-11-5 ammonium thiocyanate 
• 2234-16-4 1-(2,4-dichlorophenyl)ethan-1-one 

Downstream Products

• 125488-17-7 4-(2,4-Dichlor-phenyl)-2-piperidino-thiazol 
• 128699-99-0 N,N'-Bis<4-(2,4-dichloro-phenyl)-thiazol-2-yl>-N,N'-dimethyl-1,4-diaminobutane 
• 1616866-81-9 1-[(2,4-difluorophenyl)amino]-5-(2,4-dichlorophenyl)-1,3-dihydro-2H-imidazole-2-thione 
• 1619723-70-4 5-(2,4-dichlorophenyl)-N-(2,4-difluorophenyl)-1H-imidazol-1-amine 
• 1616865-38-3 N-(2-chloro-4,6-difluorophenyl)-2,4-dichloro-5-(2,4-dichlorophenyl)-1H-imidazol-1-amine 
• 128699-93-4 N,N'-Bis<4-(2,4-dichloro-phenyl)-thiazol-2-yl>-N,N'-dimethyl-1,2-diaminoethane 

Relevant academic research and scientific papers

Facile access to N-thiazolyl α-amino acids from α-bromo ketones and α-amino acids

N-Substituted 2-aminothiazoles are synthesized in a one-pot procedure using readily available α-bromo ketones and amines. This method is compatible with a wide range of functional groups and offers a facile and efficient access to the class of N-thiazolyl

Efficient α-thiocyanation of ketones using pyridinium hydrobromide perbromide

The direct α-thiocyanation of ketones with ammonium thiocyanate has been achieved using pyridinium hydrobromide perbromide under mild and neutral conditions to produce α-ketothiocyanates in excellent yields and with high selectivity. Copyright

Mild and efficient method for-thiocyanation of ketones and-dicarbonyl compounds using bromodimethylsulfonium bromide-ammonium thiocyanate

An efficient and convenient method for-thiocyanation of ketones and-dicarbonyl compounds has been developed using a reagent combination of bromodimethylsulfonium bromide (BDMS) and ammonium thiocyanate in acetonitrile. The developed method is mild and gave good yield of the products at room temperature.