155380-13-5

Usage

Uses

Used in Pesticide Industry:
Methyl(2E)-[2-(chloromethyl)phenyl](methoxyimino)acetate is used as an impurity in the production of Trifloxystrobin, a broad-spectrum foliar fungicide. Its presence in the synthesis process is significant as it can impact the overall quality and efficacy of the final product. The compound's role in the pesticide industry is to serve as a marker for the synthesis process, helping to ensure that the active ingredient meets the required standards for plant protection.
In the context of the provided materials, the primary use of methyl(2E)-[2-(chloromethyl)phenyl](methoxyimino)acetate is related to its origin as an impurity in the synthesis of the fungicide Trifloxystrobin. While it may not have direct applications in other industries, its presence and management in the pesticide industry are crucial for maintaining the effectiveness and safety of the final product used in plant protection. Further research and development may reveal additional applications or uses for methyl(2E)-[2-(chloromethyl)phenyl](methoxyimino)acetate in various fields, but as of now, its primary significance lies in its role in the pesticide industry.

Upstream product

• 42908-86-1 2-Chloromethylbenzoyl chloride 
• 773837-37-9 sodium cyanide 
• 87-41-2 2-benzofuran-1(3H)-one 

Downstream Products

• 174826-92-7 (2-Ethyl)hexyl 2-(chloromethyl)phenylglyoxylate 
• 174826-99-4 2-(2-chloromethylphenyl)-2-oxoacetamide 
• 174826-91-6 n-pentyl 2-(chloromethyl)phenylglyoxylate 

Relevant academic research and scientific papers

Kresoxim-methyl Derivatives: Synthesis and Herbicidal Activities of (Pyridinylphenoxymethylene)phenyl Methoxyiminoacetates

A series of new kresoxim-methyl derivatives, (pyridinylphenoxymethylene)phenyl methoxyiminoacetates, were synthesized and their structures were confirmed by NMR and high-resolution mass spectrometry (HRMS). Although derived from a fungicide, the bioassays indicated that several new compounds had good herbicidal activities. At 37.5 g a.i./ha, compound 5c showed 100% inhibition against Abutilon theophrasti, Amaranthus retroflexus, and Eclipta prostrata, which was better than mesotrione. Compound 5e had a broad herbicidal spectrum against broadleaf weeds. The present work indicates that 5c and 5e may serve as new candidates for potential herbicides.

Process for producing alkoxyiminoacetamide derivatives

A process for producing a compound of the formula (I): STR1 wherein R is hydrogen or an alkyl group, and R3 and R4 are hydrogen or an alkyl group, which comprises reacting a compound of the formula (II): STR2 wherein R1 is an optionally substituted alkyl

Preparation of halomethylbenzoyl cyanides

Halomethylbenzoyl cyanides I where Ph is phenyl which is substituted by chloromethyl or bromomethyl and may cary 1-4 other rradicals, are prepared from halomethylbenzoyl chlorides II by reacting II with a cyanide-donating compound in the presence

Preparation of halomethylbenzoyl cyanides and novel halomethylbenzoyl cyanides

A process for preparing halomethylbenzoyl cyanides I (Ph=phenyl radical substituted by chloromethyl or bromomethyl which, if desired, can additionally carry 1-4 further radicals) by reacting halomethylbenzoyl chlorides II with an alkali metal cyanide or t