36715-58-9

Upstream product

• 98-01-1 furfural 
• 99-90-1 para-bromoacetophenone 
• 108-86-1 bromobenzene 

Downstream Products

• 686725-74-6 3-(4-bromo-phenyl)-5-furan-2-yl-4,5-dihydro-pyrazole-1-carbothioic acid amide 
• 1141-60-2 (2E)-3-(furan-2-il)-1-(4-hidroxifenil)prop-2-en-1-ona 
• 61833-73-6 (4-bromo-phenyl)-(4-furan-2-yl-4,5-dihydro-1H-pyrazol-3-yl)-methanone 
• 328087-60-1 2-amino-6-(4-bromo-phenyl)-4-furan-2-yl-nicotinonitrile 
• 400031-65-4 2-amino-6-(4-bromo-phenyl)-4-furan-2-yl-nicotinamide 
• 400031-83-6 7-(4-bromo-phenyl)-5-furan-2-yl-3-(2-methoxy-phenyl)-2-thioxo-2,3-dihydro-1H-pyrido[2,3-d]pyrimidin-4-one 
• 328087-64-5 4-amino-7-(4-bromo-phenyl)-5-furan-2-yl-1H-pyrido[2,3-d]pyrimidine-2-thione 
• 1246226-96-9 2-(3-(4-bromophenyl)-1-(furan-2-yl)-3-oxopropylthio)acetic acid 
• 1279691-21-2 3-(4-bromophenyl)-5-(2-furyl)-4,5-dihydropyrazole-1-carboxamide 
• 1384263-28-8 methyl 2-(3-(4-bromophenyl)-1-(furan-2-yl)-3-oxopropylthio)acetate 
• 1109280-76-3 C₁₄H₁₀BrN₃O 

Relevant academic research and scientific papers

Novel 4,5-dihydro-1H-pyrazole derivatives as potential succinate dehydrogenase inhibitors: design, synthesis, crystal structure, biological activity and molecular modeling

Twenty-eight new 4, 5-dihydro-1H-pyrazole derivatives were designed, synthesized and characterized by IR, 1H NMR, 13C NMR and HRMS. The crystal structure of compound 2j was characterized by single crystal X-ray diffraction. Their ant

Design, synthesis, and antifungal activity evaluation of novel 2-cyano-5-oxopentanoic acid derivatives as potential succinate dehydrogenase inhibitors

Two series of novel 2-cyano-5-oxopentanoic acid derivatives (1a?l, 2a?l) were designed, synthesized, and characterized by IR, 1H NMR, 13C NMR, and HRMS. Their in vitro antifungal activity against five plant pathogenic fungi were then

Design, synthesis and insecticidal activity of novel semicarbazones and thiosemicarbazones derived from chalcone

Thirty semicarbazone and thiosemicarbazone derivatives (2a–w and 4a–g) from chalcones containing furan and thiophene ring were designed and synthesized. They were characterized by IR, 1H NMR, 13C NMR and HRMS. The crystal structure o

6-methoxypyridine derivative and application thereof in pesticide

The invention relates to a 6-methoxypyridine derivative and application thereof in pesticides, which belong to the technical field of pesticides. The structural formula of the 6-methoxyl pyridine derivative is shown as a formula (I), and in the formula (I

Transition metal-free domino aryl-aryl coupling/phospha-Michael addition of diarylphosphinite to α,β-unsaturated ketones triggered by alkaline hydrolysis of (4-(2-alkenoyl)phenyl)triarylphosphonium salts

Alkaline hydrolysis of a variety of (4-(2-alkenoyl)phenyl)triarylphosphonium bromides is reported. This hydrolysis triggers coupling of 4-(2-alkenoyl)phenyl with one aryl via phosphorus(V). Both diarylphosphinite and an α,β-unsaturated ketone are in situ generated and then undergo phospha-Michael addition to provide β-diarylphosphoryl ketones bearing a biaryl moiety in 27–70% yields in the absence of a transition metal.

4, 5-dihydropyrazole compound and application thereof in pesticides

The invention relates to a 4, 5-dihydropyrazole compound and an application thereof in pesticides, which belong to the technical field of pesticides. The technical problem to be solved by the invention is to provide a new compound which can be used as an

Studies of NMR Chemical Shifts of Chalcone Derivatives of Five-membered Monoheterocycles and Determination of Aromaticity Indices

A series of the chalcone derivatives of the five-membered monoheterocyclic compounds, (E)-1-aryl-3-heteroarylpropen-1-ones, were prepared by aldol condensation of the corresponding aldehydes of thiophene, pyrrole, and furan with m- and p-substituted acetophenones. Similar condensation of the acetyl compounds of the heterocycles with m- and p-substituted benzaldehydes gave another series of the chalcone derivatives, (E)-1-heteroaryl-3-arylpropen-1-ones. The 13C chemical shift values (δC) of the chalcone derivatives were determined in order to find if they correlated with the Hammett σ values. A good correlation, especially for the β-C for both series, was found for the 13C chemical shift values (δC) of the chalcone derivatives with the Hammett σ values. The chemical shift values of the β-C of the heterocyclic compounds were plotted against those of the benzene derivatives. The resulting slopes were found to be close to the values of the aromaticity indices.

1-(2-furyl)-3-(4-substituted phenyl)propylene derivative as well as preparation method and application thereof

The invention provides a 1-(2-furyl)-3-(4-substituted phenyl)propylene derivative as well as a preparation method and application thereof. The derivative has a structural formula (I) shown in the following description; in the structural formula (I), R is

3-(2-furyl)propenol derivative as well as preparation method and application thereof

The invention provides a 3-(2-furyl)propenol derivative as well as a preparation method and application thereof. The derivative has a structural formula (I) shown in the following description; in the structural formula (I), R is a fluorine atom, a chlorin

Semicarbazone compound and preparation method and application thereof

The invention provides a semicarbazone compound and a preparation method and application thereof. The structural general formula of the compound is shown in the description, wherein the R represents fluorine atoms, chlorine atoms, bromine atoms, iodine at