2009Unpublished venueRequires access

Synthesis and Molluscicidal Activity of Phoxim Analogues

Zhao Qing-xia

Open publisher page 0 citations

Abstract

In order to search for novel more effective and less toxic molluscicides,nine new phoxim analogues(2a-2i) were synthesized from substituted phenylacetonitriles by oximation and thiophosphorylation. All compounds were confirmed by elemental analyses,IR,1HNMR and MS. Preliminary biological screening showed that compounds 2a,2b and 2h appeared to have significant molluscicidal activity against Oncomelanis hwpensis snails. The LC50 of the compounds 2a,2b and 2h against snails were 0.31,0.33 and 0.38 mg/L,respectively.

About this research paper

What this paper is about

In order to search for novel more effective and less toxic molluscicides,nine new phoxim analogues(2a-2i) were synthesized from substituted phenylacetonitriles by oximation and thiophosphorylation. All compounds were confirmed by elemental analyses,IR,1HNMR and MS. Preliminary biological screening showed that compounds 2a,2b and 2h appeared to have significant molluscicidal activity against Oncomelanis hwpensis snails. The LC50 of the compounds 2a,2b and 2h against snails were 0.31,0.33 and 0.38 mg/L,respectively.

Why it matters

A significance statement is not available in the OpenAlex record.

Key contribution

A contribution statement is not available in the OpenAlex record.

Method / approach

Method details are not available in the OpenAlex metadata.

Main findings

Findings are not separately available in the OpenAlex metadata.

Limitations

Limitations are not available in the OpenAlex metadata.

Applications

Application details are not available in the OpenAlex metadata.

Available abstract

In order to search for novel more effective and less toxic molluscicides,nine new phoxim analogues(2a-2i) were synthesized from substituted phenylacetonitriles by oximation and thiophosphorylation. All compounds were confirmed by elemental analyses,IR,1HNMR and MS. Preliminary biological screening showed that compounds 2a,2b and 2h appeared to have significant molluscicidal activity against Oncomelanis hwpensis snails. The LC50 of the compounds 2a,2b and 2h against snails were 0.31,0.33 and 0.38 mg/L,respectively.

Key concepts: Phoxim, Chemistry, Pesticide, Toxicology, Stereochemistry, Biology, Ecology

Related papers

Back to paper searchBrowse research topicsOriginal source
Synthesis and Molluscicidal Activity of Phoxim Analogues — Research Paper | ScholarLens