The present invention provides a compound having an excellent efficacy for controlling pests A tetrazolinone compound of a formula (1): [wherein R1 represents an C6-C16 aryl group, an C1-C12 alkyl group, or a C3-C12 cycloalkyl group, etc, which each optionally be substituted; R2, R3, R4 and R5 represent independently of each other a hydrogen atom, a halogen atom or an C1-C3 alkyl group, etc; R6 represents an C1-C6 alkyl group, a C3-C6 cycloalkyl group, a halogen atom, a C1-C6 haloalkyl group, an C2-C6 alkenyl group, an C1-C6 alkoxy group, or a C1-C6 haloalkoxy group, etc; R7, R8 and R9 represent independently of each other a hydrogen atom, a halogen atom, or an C1-C4 alkyl group, etc; X represents an oxygen atom or a sulfur atom; and R10 represents an C1-C6 alkyl group, etc] shows an excellent controlling efficacy on pests

Tetrazolinone compounds and their use as pesticides

The present invention relates to the use of strobilurine type compounds of formula I and the N-oxides and the salts thereof for combating phytopathogenic fungi containing a mutation in the mitochondrial cytochrome b gene conferring resistance to Qo inhibitors, and to methods for combating such fungi. The invention also relates to novel compounds, processes for preparing these compounds, to compositions comprising at least one such compound, to plant health applications, and to seeds coated with at least one such compound.

Use of strobilurin type compounds for combating phytopathogenic fungi resistant to qo inhibitors

A plant disease control composition comprising a carboxamide compound represented by following formula (I), wherein R1 represents a hydrogen atom or a methyl group, and R2 represents a methyl group, a difluoromethyl group or a trifluoromethyl group, and fludioxonil is provided by this invention, and this composition has an excellent effect for controlling plant disease.

Plant disease control composition and its use

The invention concerns benzoyl derivatives of formula (I) in which the variables have the following meanings: R1, R2: hydrogen, nitro, halogen, cyano, alkyl, alkyl halide, alkoxy, alkoxy halide, alkylthio, alkylthio halide, alkylsulphinyl, alkylsulphinyl halide, alkylsulphonyl, or C?1?-C6 alkylsulphonyl halide; R?3?: hydrogen, halogen or alkyl; R4, R5: hydrogen, halogen, cyano, nitro, alkyl, alkoxy, alkylthio, dialkylamino, phenyl or carbonyl, wherein the six last-mentioned groups can be substituted; X: O, S, NR9, CO or CR10R11; Y: O, S, NR12, CO or CR?13R14; R15?: optionally substituted pyrazole which is bonded in position 4 and carries a hydroxy or sulphonyloxy group in position 5. The invention also concerns: the salts of these 3-heterocyclyl-substituted benzoyl derivatives which can be used for agricultural purposes; processes and intermediate products for preparing these substances; agents containing them; and the use as herbicides of these derivatives or agents containing them.

3-heterocyclyl-substituted benzoyl derivatives

The invention belongs to the organic synthesis field, and provides a preparation method of a substituted pyrazolylether compound having a structure represented by formula I The method comprises the following reaction steps: 1, reacting a compound II with an alkali in the presence of a polar solvent to prepare the metal salt of the compound II, and removing the polar solvent; 3, adding an organic solvent and a compound III to the compound II, heating to a temperature in a range of 20DEG C - the reflux temperature of the organic solvent in the presence of an organic/inorganic catalyst to prepare a crude compound I, and removing the organic solvent; and 3, adding an extracting agent and water to a reaction system, layering, steaming out the extracting agent in the obtained organic layer to obtain a crude compound I, adding a recrystallization solvent for recrystallization to obtain the compound I, wherein a reaction equation in step 2 is shown in the specification, and all groups in the reaction equation are defined in the specification The preparation method has the advantages of avoiding of the generation of a byproduct N-alkylated isomer, high yield and high purity of the obtained product, cost reduction, reduction of the influences to the surrounding environment, and suitableness for the industrialization

Preparation method of substituted pyrazolylether compound

The invention relates to 2-[pyrazolyl and triazolyl-3'-oxymethylene]-phenyl-isoxazolones, triazolones and tetrazolones of formula (I), wherein the indices and the substituents have the following meaning: X represents a group A, B or C, # indicating the bond with the phenyl ring, Ra being hydrogen, halogen, alkyl or alkoxy and Rb being alkyl; Y represents N or CRc, Rc being hydrogen, halogen or alkyl; n represents 0, 1, 2, 3 or 4 and the substituents R1 can be different when n is greater than 1; R1 represents nitro, cyano or halogen, optionally substituted alkyl or optionally substituted alkoxy or if n is 2, additionally an optionally substituted bridge which is bound to two adjacent ring atoms, said bridge containing three to four members from the group of 3 or 4 carbon atoms, 2 to 3 carbon atoms and 1 or 2 nitrogen, oxygen and/or sulphur atoms, and together with the ring to which it is bound may form a partially unsaturated or aromatic radical; R2 represents hydrogen, nitro, cyano, halogen, alkyl, halogenalkyl, alkoxy, alkylthio or alkoxycarbonyl and R3 represents optionally substituted alkyl, optionally substituted cycloalkyl, optionally substituted aryl or optionally substituted hetaryl.

2-[pyrazolyl and triazolyl-3'-oxymethylene]-phenyl-isoxazolones, triazolones and tetrazolones as pesticides and fungicides

The present invention relates to a process for preparing a pyridazine amine compound of formula V, and to processes for preparing dichloropyridazine amine compounds of formula IVa, IVb, or mixtures thereof. Furthermore, the present invention relates to the novel dichloropyridazine amine compounds of formula IVa, IVb,ormixtures thereof, wherein the amino group is an ethylamino group.

Process for preparing 4-amino-pyridazines

The present invention relates to a process for the preparation of limonene-4-ol by an epoxide ring opening isomerization of terpinolene epoxide.

Process for the preparation of limonene-4-ol

The present invention relates to a catalytic process for preparing pyrazoles comprising the step of cyclizing hydrazone substituted α,β-unsaturated carbonyl compounds by reacting them with hydrogen in a reaction mixture comprising as components (a) a hydrogenation catalyst, (b) an acid selected from Bronsted acids, ammonium salts of Bronsted acids, and Lewis acids, (c) a protic solvent, and optionally (d) an aprotic solvent.

Catalytic hydrogenation process for preparing pyrazoles

The present invention relates to a process for preparing a mixture of terpene alcohols comprising limonene-4-ol and terpinene-4-ol from terpinolene epoxide via an isomerization and/or hydrogenation reaction in the presence of a copper catalyst.

Process for preparing a mixture of terpene alcohols

Handle everyday research tasks with reliable, citation-backed results

Your personal Research Agent to handle research tasks with citation-backed results

Popular Tasks used by Researchers

How can I help with your research?

Meet SciSpace

Get more enhanced response by uploading the PDFs you want me to reference.

No relevant PDFs in your library

SciSpace is the AI research assistant for academics. Run systematic literature reviews on 280M+ papers, and write papers with cited sources. Trusted by 1M+ students, PhDs & researchers.

SciSpace | AI for Research

Analyze PDFs

Code & Manuscripts

Funding & Grants

Literature & Patents

Medical & Clinical Data

Systematic Review

Visualize & Present

Web & Data

Build a Google Scholar-like website for your research.

Build a website

Create charts and images for your research

Create a Chart

Write a paper for submission to a journal

Draft a manuscript

Patent Search

Design eye-catching scientific posters in minutes.

Scientific Poster Generation

Systematic Literature Review

One task is running at the moment. Your messages will be shown right after.

Drag and drop or click here to browse

Loved by <highlight>1 million+</highlight> researchers

Extract a list of specific topics and their sources from unstructured text

Topics

Compare and analyze relevant papers that matches with your search

Papers

Get insights from PDFs and bookmarked papers from your library

My library

Recent searches

Try searching for:

Catch AI-generated content in scholarly and non-scholarly content

{ai} Detector

Ai Writer

Get PDF Summaries, highlighted text explanations 

Chat with PDF

Effortlessly create in-text citations and bibliographies in APA and 2,500 other formats

Citation generator

Get explanations, summaries, and answers on academic papers

Ease up your research workflow with {scispace}'s cohort of exciting AI tools

Elevate your academic writing skills and convey your ideas the way you want

Paraphraser

Explore our range of reading and writing tools

Your file is being prepared and should be ready in a few minutes. If it's a large file, it might take a bit longer. You can close this window, and we'll email you the file when it's done.

You have reached a maximum limit of <strong>{limit}</strong> columns in the table. Remove at least <strong>1</strong> column to add or create another one.

Goetz Roland

Author Tools

Chat about Author