55606-45-6

Upstream product

• 7647-01-0 hydrogenchloride 
• 3717-26-8 2-chlorobenzaldoxime 
• 7440-44-0 pyrographite 
• 620-20-2 1-Chloro-3-chloromethyl-benzene 
• 89-98-5 2-chloro-benzaldehyde 
• 18099-45-1 diborane 

Downstream Products

• 81777-71-1 3-chloro-N-(2-chlorobenzyl)-N-hydroxy-2,2-dimethyl-propionamide 

Relevant academic research and scientific papers

Method for producing carbendazim by electrodialysis method and production device thereof (by machine translation)

The apparatus, disclosed by the invention comprises a bipolar membrane electrodialysis reactor and a reaction kettle, bipolar membrane electrodialysis reactor which are further, communicated with sulfuric acid tank and hydrochloric acid tank N - (2 - to generate) - chlorine (N-benzyl, N - (2 - hydroxylamine) - chlorine-benzyl, hydroxyl - 2222, 2-dimethyl-propionamide, chloride - N N N N N-Bethanesulfonyl chloride, for generating and killing methyl 3 - hydroxyl - 2222,2-dimethyl-propionamide under alkaline condition is produced) - N - chlorine - N N N N N-propionamide under alkaline condition.3 - The production device disclosed by the, invention has the advantages of high, production efficiency) - N - yield, high, product quality; and the like in the electrolysis process, discloses a bipolar membrane electrodialysis reaction method, and a bipolar membrane electrodialysis reaction, still, liquid, produced by using a bipolar membrane electrodialysis, method and a double-polar membrane electrodialysis reactor. (by machine translation)

Antimicrobial N-(2-chlorobenzyl)-substituted hydroxamate is an inhibitor of 1-deoxy-d-xylulose 5-phosphate synthase

N-(2-Chlorobenzyl)-substituted hydroxamate, readily produced by hydrolysis of ketoclomazone, was identified as an inhibitor of 1-deoxy-d-xylulose 5-phosphate synthase (DXS), with an IC50 value of 1.0 μM. The compound inhibited the growth of Haemophilus influenzae. A convenient spectroscopic method for assaying DXS using NADPH-lactate dehydrogenase (LDH) is also reported.

Herbicidal 3-isoxazolidinones and hydroxamic acids

Novel 3-isoxazolidinone compounds and novel hydroxamic acid intermediates from which they are prepared exhibit herbicidal activity to grassy and broad-leaf plant species while leaving legumes, especially soybeans, unaffected. The preparation and herbicidal activity of the compounds is exemplified.

Herbicidal isoxazolidine-3,5-diones

2-Substituted isoxazolidine-3,5-diones and isoxazolidine-3-one-5-thiones exhibit herbicidal activity, controlling effectively the growth of a wide spectrum of grassy and broad-leaved plant species. The preparation and herbicidal activity of the compounds is exemplified.