cas 312920-05-1|| where to buy (2Z)-2-[(2,1,3-benzoxadiazol-4-yl)imino]-6,8-dibromo-N-[(furan-2-yl)methyl]-2H-chromene-3-carboxamide

Nombre del producto:(2Z)-2-[(2,1,3-benzoxadiazol-4-yl)imino]-6,8-dibromo-N-[(furan-2-yl)methyl]-2H-chromene-3-carboxamide

IUPAC Name:(2Z)-2-[(2,1,3-benzoxadiazol-4-yl)imino]-6,8-dibromo-N-[(furan-2-yl)methyl]-2H-chromene-3-carboxamide

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: Núm. De CAS :312920-05-1; Fórmula molecular:C21H12Br2N4O4; Punto de fusión:-; Código de sonrisas:BrC1=CC(Br)=C2O\C(=N/C3=CC=CC4=NON=C34)C(=CC2=C1)C(=O)NCC1=CC=CO1; Densidad:

: Número de catálogo:CM777793; Peso molecular:544.16; Punto de ebullición:; Nº Mdl:; Almacenamiento:

: Furans; Furan is a cyclic flammable liquid compound C4H4O that is obtained from wood oils of pines or made synthetically and is used especially in organic synthesis. Furan is aromatic because a pair of lone pair electrons of the oxygen atom in its molecule forms a large π bond in the plane of the conjugated orbital, making a total of 6 electrons in the plane of the conjugated plane, conforming to the 4n+2 structure. Aromaticity makes furan have the property of easy substitution and difficult addition. The other lone pair of electrons in oxygen stretches out. The oxygen atom itself conforms to sp2 hybridization. Due to the presence of the aromatic ring, the chemical behavior of furan is not very similar to that of other unsaturated heterocycles. The oxygen in the aromatic ring has an electron-donating effect, so the electrophilic substitution reactivity of furan is stronger than that of benzene.; Furan | C4H4O | Where to Buy Furans-Chemenu; Furane | Furanes | Furfuran | Furan | C4H4O | Furan Synthesis | Where to Buy Furans; Looking to buy furan? Chemenu offers a diverse selection of high-quality furan compounds. Find the perfect furans for your research or industrial applications. Explore our inventory today!

: Benzofurazans; Benzofurazans are important pharmaceutical intermediates. Benzofurazans are known bioisosteres of the nitro group. Both oxadiazoles and nitro groups have strong electron-withdrawing properties, but when optimizing drug-like properties such as activity, selectivity, and stability, the absence of standard charges in the oxadiazole structure may be more beneficial to drug products. What's more, nitro groups have been identified as toxic groups, and it is routine to remove or replace them in the early stages of drug development.