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Méthode de broyage du 2-amino benzo f chromène

2-Amino-4-phenyl-4H-benzo [h]chromene-3-carbonitrile

2-Amino-4-phenyl-4H-benzo[h]chromene-3-carbonitrile | C20H14N2O | CID 3121293 - structure, chemical names, physical and chemical properties, classification, patents, literature, biological activities, safety/hazards/toxicity information, supplier lists, and more.

Crystal structure of 2-amino-4-phenyl-4H-benzo[h]chromene …

In the title compound, C 20 H 14 N 2 O, the plane of the phenyl ring is almost normal to that of the naphthalene ring system, forming a dihedral angle of 83.15 (8)°. The 4H-pyran ring fused with the naphthalene ring system has a flattened boat conformation.In the crystal, mol­ecules are linked by pairs of N—H⋯N hydrogen bonds, forming inversion dimers …

Synthetic strategies and pharmacological activities of chromene …

Synthesis, Cytotoxic Activity, Crystal Structure, DFT Studies and Molecular Docking of 3-Amino-1-(2, 5-dichlorophenyl)-8-methoxy-1H-benzo [f] chromene-2-carbonitrile. Crystals (2021) ... hydroxyapatite from green mussel shell waste combined with CoFe 2 O 4 as a heterogeneous catalyst for synthesizing 2-amino-4H-chromene derivative. The green ...

Crystal structure of 3-amino-1-(4-meth-oxy-phen-yl)-1H-benzo[f]chromene …

In the title compound, C21H16N2O2, the meth-oxy-benzene ring is almost perpendicular to the mean plane of the naphthalene ring system, making a dihedral angle of 83.62 (5)°. The 4H-pyran ring fused with the naphthalene ring system is almost planar [maximum deviation = 0.033 (1) Å]. In the crystal, m …

Synthesis, in-vitro cytotoxicity of 1H-benzo [f]chromene …

A series of 1 H -benzo[ f ]chromene-2-carbonitriles was synthesized and evaluated for their cytotoxic activities against MCF-7, HCT-116, and HepG-2 cancer cells. The SAR studies reported that the substitution in the phenyl ring at 1-position of 1 H -benzo[ f ]chromene nucleus with the specific group, H atom, or methoxy group at 9-position increases the …

Enantioselective synthesis of 3‐amino‐1‐aryl‐1H‐benzo[f]chromene‐2 …

A novel chiral magnetic nanocatalyst was prepared by the surface modification of Fe 3 O 4 magnetic nanoparticles (MNPs) with a chloropropylsilane and further by arginine to form Fe 3 O 4 @propylsilan-arginine (Fe 3 O 4 @PS-Arg). After the structural confirmation of Fe 3 O 4 @PS-Arg synthesized MNPs by Fourier transform-infrared, X-ray diffraction, field …

3-Amino-1-phenyl-1H-benzo[f]chromene-2-carbonitrile

3-Amino-1-phenyl-1H-benzo[f]chromene-2-carbonitrile Acta Crystallogr Sect E Struct Rep Online. 2013 Mar 1;69(Pt 3):o401. doi: 10.1107/S1600536813004376. Epub 2013 Feb 20. Authors Mehmet Akkurt 1, Alan R Kennedy, Shaaban Kamel Mohamed, Sabry H H Younes, Gary J Miller. Affiliation 1 Department of Physics ...

Green methods mediated synthesis of chromene

Fast and efficient green procedure for the synthesis of benzo[5,6]Chromene derivatives and their sulfur analogues in water by organocatalyst potassium phthalimide- N -oxyl ... cyclic 1,3-diketone, and 1,3-C,N-binucleophiles such as 2-amino-1,4-naphthoquinone or 4-aminocoumarin in PEG-200 as solvent provided the styryl-linked naphthoquinone ...

Procédés de broyage / Processium

Le broyage peut mettre en jeu différents mécanismes : la compression (écrasement), l'impact (percussion), la coupure (cisaillement) et l'attrition (frottement) qui impacte les …

Préparation d'échantillons

Broyage par impact de billes. Oscillations verticales de 500 à 2000 oscill/min. Capacité : 4 microplaques de 96 puits ou 16 tubes 50 mL. Broyage rapide en moins de 3 min. …

Broyage dans les industries agroalimentaires

5. Applications du broyage aux industries agroalimentaires. Dans les industries agricoles et alimentaires, le broyage est une opération unitaire très répandue. Tous les types de …

Méthodes d'élaboration de matériaux

On étudie la variation de avec le pH du milieu. Bonne stabilité: de même signe et supérieur à 20 mV en valeur absolue pour chaque poudre. Mesures souvent complétées par des …

Convenient and Efficient One-Pot Method for the Synthesis of 2-Amino

Abstract. A convenient and efficient one-pot method for the synthesis of 2-amino-tetrahydro-4H-chromene and 2-amino-4H-benzo[h]-chromene derivatives has been developed using a catalytic amount of amino-functionalized MCM-41 in aqueous medium.This efficient technique has the advantages of giving 4H-tetrahydro-chromene …

Synthesis of 6H-benzo[c]chromene as a new electron-rich …

Synthesis of 6H-benzo[c]chromene as a new electron-rich building block of conjugated alternating copolymers and its application to polymer solar cells J. W. Lee, S. Bae and W. H. Jo, J. Mater. Chem. A, 2014, 2, 14146 DOI: 10.1039/C4TA02929A

Synthesis of halogen derivatives of benzo[h]chromene and benzo…

The synthesis of novel 7-(4-halophenyl)-8,9-dihydro-7H-12-oxa-9,11-diaza-benzo[a]anthracene derivatives has been reported. The key intermediate 3-amino-9-chloro-1-(4-halophenyl)-1H-benzo[h]chromene-2-carbonitrile (3) was obtained by treating 4-halobenzylidenmalononitriles (1a-c) and ethyl 4-halobenzylidenmalonates (1d-f) with 4 …

(IUCr) Crystal structure of 2-amino-4-phenyl-4H-benzo[h]chromene …

For the crystal structure of the isomer of the title compound, 3-amino-1-phenyl-1H-benzo[f]chromene-2-carbonitrile, see: Akkurt et al. (2013). Experimental top. To a solution of 1-naphthol (144 mg; 1 mmol) in 10 ml absolute ethanol, an equimolar amount of benzylidene-malononitrile (154 mg; 1 mmol) was added with constant stirring. The …

2H/4H-Chromenes—A Versatile Biologically Attractive Scaffold

Introduction. Bicyclic oxygen heterocycles-containing a benzene fusion ring at a 5,6-positioned 4H-pyran ring system designated as 4H-chromene (4H-ch) has attracted considerable attention as an important structural motif for the discovery of new drug candidates (El-Gaby et al., 2000).Four common structure motifs are formed, which …

One-step synthesis of substituted 2-amino-4H-chromenes and 2-amino …

Substituted 2-aminochromenes were synthesized by three-component condensation of aromatic aldehydes, derivatives of cyanoacetic acid, and phenols or naphthols. The molecular and crystal structure of 2-amino-3-cyano-6-hydroxy-4-phenyl-4H-benzo[f]chromene was established by X-ray diffraction analysis.

3-IMINO-3H-BENZO (F)CHROMENE-2-CARBOXAMIDE

3-IMINO-3H-BENZO(F)CHROMENE-2-CARBOXAMIDE AldrichCPR; CAS Number: 2; Linear Formula: C14H10N2O2; find -R582972 MSDS, related peer-reviewed papers, technical documents, similar products & more at Sigma-Aldrich

Green and Mechanochemical One-Pot Multicomponent …

technology for the synthesis of 2-amino-4H-benzo[b]pyrans using amine-functionalized silica magnetic nanoparticles (NH 2 @SiO 2 @Fe 3 O 4). In the last few years, tetrahydrobenzo- ...,17 ethyl-2-(2-amino-6-bromo-3-cyano-4H-chromene-4-yl)-2-cyanoacetate (C),10 2-amino-7-(dimethylamino)-4-(4-(dimethylamino)naphthalene-

Quel est le but de broyage processus?

2.Becauseof l'exploitation minière et de broyage chantier de la taille du produit final d'enquêter afin de s'assurer que l'usine de test pendant au représentant mine. 3. Pour le …

l-Cysteine functionalized magnetic nanoparticles (LCMNP…

The applicability of the LCMNP material was evaluated in a three-component coupling reaction between a nucleophile, salicylaldehyde and malononitrile as the catalyst for one-pot synthesis of 2-amino-4H-chromene-3-carbonitrile derivatives. The catalyst system showed high catalytic activity in this process and target products were obtained in ...

2-AMINO-4-PHENYL-4H-BENZO (H)CHROMENE-3-CARBONITRILE

2-AMINO-4-PHENYL-4H-BENZO(H)CHROMENE-3-CARBONITRILE AldrichCPR; CAS Number: 11; Linear Formula: C20H14N2O; find -R424196 MSDS, related peer-reviewed papers, technical documents, similar products & more at Sigma-Aldrich ... 3-AMINO-1-(3-HYDROXY-PHENYL)-1H-BENZO(F)CHROMENE-2-CARBONITRILE. …

Chromene

Reactions performed in the presence of nano-CuFe 2 O 4 as catalyst and water as solvent afforded the corresponding 2-amino-4H-chromene-4-carboxylates and 2-amino-5H-pyrano[3,2-c]chromene-4-carboxylates in presentable yields (Scheme 6). The nanocatalyst can be reused for six cycles without any significant reduction in product yield.