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The introduction of fluorine into bioactive molecules is a matter of importance in medicinal chemistry. In this study, representatives of various chemical entities of fluoroaromatic compounds were synthesized. Depending on the reaction conditions, either tetrafluorophthalimides or ammonium tetrafluorophthalamates are accessible from tetrafluorophthalic anhydride and primary amines. Tetrafluorophthalamic acids undergo thermal decarboxylation to yield tetrafluorobenzamides. These could be successfully converted upon treatment with primary amines, in the course of an aromatic nucleophilic substitution, to 2,3,5-trifluorobenzamides with respective amino substituents at the 4-position. The five structure types were characterized by means of spectroscopic and crystallographic methods. The synthesized compounds were evaluated as inhibitors of angiogenesis by measuring microvessel outgrowth in a rat aortic ring assay. The biological activity was maintained throughout these different polyfluorinated chemotypes.

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Reference:
Benzofuran – Wikipedia,
Benzofuran | C8H3766O – PubChem

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A specific example of a Sequestration Enabling Reagent (SER), tetrafluorophthalic anhydride, is used in the purification of solution-phase reactions involving amines with electrophiles. The SER is added to an incomplete reaction mixture containing product, amine, and electrophile. The SER covalently reacts with remaining amine, affording a derivatized amine with an artificially-imparted acid tag. This ‘tagged’ amine is now sequesterable by the same CMR/R polyamine resin used to sequester the electrophile and both are easily removed from the reaction mixture affording pure product.

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Reference:
Benzofuran – Wikipedia,
Benzofuran | C8H3751O – PubChem

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In this paper we report the design, synthesis and pharmacological evaluation of a new series of phenyl sulfonamide derivatives 2a-h and 3-8 planned by structural modification on the anti-inflammatory prototype LASSBio-468 (1). Among the synthesized analogues, the tetrafluorophthalimide LASSBio-1439 (2e) stands out showing an in vitro anti-TNF-a effect similar to the standard thalidomide. The relevance of tetrafluorination of the phthalimide nucleus was also confirmed by the anti-inflammatory profile of 2e, through oral administration, in a murine model of pulmonary inflammation. The corresponding tetrafluorocarboxyamide metabolite LASSBio-1454 (15), generated from partial hydrolysis of the derivative 2e, presented a significant in vitro effect and a pronounced anti-inflammatory activity in vivo.

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Reference:
Benzofuran – Wikipedia,
Benzofuran | C8H3717O – PubChem

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Fluorescence microscopy reveals the localization, spatial distribution, and temporal dynamics of the specifically labeled organelles in living cells. Labeling with exogenous conjugates prepared from fluorescent dyes and small molecules (ligands) is an attractive alternative to the use of fluorescent proteins, but proved to be challenging due to insufficient cell-permeability of the probes, unspecific staining, or low dye brightness. We evaluated four green-emitting rhodamine dyes and their conjugates intended for the specific labeling of lysosomes, mitochondria, tubulin, and actin in living cells. The imaging performance of the probes in living human fibroblasts has been studied by using confocal and stimulated emission depletion (STED) super-resolution microscopy with a commercial 595 nm STED laser. Two bright and photostable dyes (LIVE 510 and LIVE 515) provide specific and versatile staining.

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Reference:
Benzofuran – Wikipedia,
Benzofuran | C8H3722O – PubChem

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Benzylphthalimide analogs (P1P’s) and phenethylphthalimide analogs (P2P’s) have been found to exhibit thalidomide-like activity on the production of tumor necrosis factor (TNF)-alpha by the human leukemia cell line, HL-60, stimulated by 12-O-tetradecanoylphorbol-13-acetate (TPA). Structure-activity relationships are discussed on the basis of the TNF-alpha production-enhancing activity. Benzylphthalimide (P1P-00) exhibited activity which is weaker than that of thalidomide, but introduction of a methyl group at the ortho-position of the benzyl moiety (P1P-10) resulted an increase to a level comparable with that of thalidomide. Phenethylphthalimide (P2P-00) is more potent than thalidomide, and its fluorinated derivative, 2-phenethyl-4,5,6,7-tetrafluoro- 1H-isoindole-1,3-dione (FP2P-00), exhibited potent activity at very low concentrations.

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Reference:
Benzofuran – Wikipedia,
Benzofuran | C8H3760O – PubChem

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Novel highly fluorinated polyimides containing hexafluoronaphthylene fragment in the main chain were prepared by the two-stage polymerization of 2,7- and 2,6-diaminohexafluoronaphthalenes with 4,4?-oxydiphthalic anhydride: polycondensation in a solution at 80 C followed by high-temperature solid-state chain extension. The influence of hexafluoronaphthylene fragment isomerism on the key polyimide features – molecular weight, thermal stability, solubility, optical properties – was characterized. Polyimides based on 2,7-diaminohexafluoronaphthalene or easily accessible mixture of isomeric diamines formed the flexible, transparent, and thermostable films.

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Reference:
Benzofuran – Wikipedia,
Benzofuran | C8H3763O – PubChem

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Structurally modified phthalimide derivatives were prepared through condensation of phthalic and tetrafluorophthalic anhydride with selected sulfonamides with variable yields. All compounds were screened for their antimycobacterium activity against Mycobacterium tuberculosis H37Ra (ATCC 25177) using a micro broth dilution technique. The fluorinated derivatives (compounds 2c, 2d, 2f and 2h) had antimycobacterium activity comparable with classical sulfonamide drugs. The minimum inhibitory concentration (MIC) of compounds 2c, 2d, 2f and 2h was greater than that of isoniazid (MIC <0.02 mug/mL) and in vitro activity was greater than that of pyrazinamide, another first line antimycobacterium drug (MIC 50-100 mug/mL). The new compounds could be considered new lead compounds in the treatment of multi-drug resistant tuberculosis. Note that a catalyst decreases the activation energy for both the forward and the reverse reactions and hence accelerates both the forward and the reverse reactions.Product Details of 652-12-0, you can also check out more blogs about652-12-0

Reference:
Benzofuran – Wikipedia,
Benzofuran | C8H3700O – PubChem

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PROBLEM TO BE SOLVED: To provide a coloring composition for a color filter which is excellent in brightness, contrast, and heat resistance, and to provide a color filter. SOLUTION: The coloring composition for a color filter contains: a pigment containing a quinophthalone compound represented by the following formula; a binder resin; an organic solvent; and a photopolymerizable monomer and/or a photopolymerization initiator. The color filter includes a filter segment formed of the coloring composition for a color filter. SELECTED DRAWING: None COPYRIGHT: (C)2016,JPO&INPIT

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Benzofuran – Wikipedia,
Benzofuran | C8H3695O – PubChem

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Fluorinated pentacene derivatives, for example, the novel compounds tetradecafluoropentacene, 5,6,7,12,13,14-hexafluoropentacene, 5,7,12,14-tetrafluoropentacene, and 6,13-difluoropentacene, and intermediates therefor are provided. And a method of producing fluorinated pentacene derivatives and intermediates therefor is also provided. Pentacene derivatives fluorinated at desired positions of the pentacene skeleton are obtained by introducing the oxo group, hydroxyl group, or alkoxyl group into the pentacene skeleton followed by fluorination with sulfur tetrafluoride and partial defluorination using a reducing agent.

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Reference:
Benzofuran – Wikipedia,
Benzofuran | C8H3687O – PubChem

Sep 2021 News Archives for Chemistry Experiments of 652-12-0

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Studies on fluorine containing condensation polymers are limited compared to that of fluorine containing addition polymers. In this report, highly fluorinated aromatic polyesters were synthesized by a polycondensation reaction of tetrafluorophthalic anhydride with ethylene glycol. Viscosity, solubility, thermal properties and crystallization behaviors of fluorinated polyesters were investigated using IR, 19F NMR, DSC, GPC, polarized optical microscope and rheometer. The fluorinated polyester is insoluble in most organic solvents, such as acetone, ethyl acetate, chloroform, THF, and trichloromethane. However, it is soluble in highly polar solvents, such as dimethylsulfoxide, dimethylformamide and dimethylacetamide. The fluorinated polyester (o-PETF) is a crystalline polymer with a crystallization enthalpy of 35.2 J/g and a broad crystallization temperature range from 54 to 130 C. Average crystalline growth rate is 4.2 mum/min at 110 C in the preliminary 30 min. Spherulite growth was observed at the temperature when the dendrites begin to melt. Crystallization property of o-PETF may be ascribed to the higher mobility of fluorinated polyester chains and dipolar contribution of carbon-fluorine bonds.

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Reference:
Benzofuran – Wikipedia,
Benzofuran | C8H3783O – PubChem