cas 2356086-93-4|| where to buy N-(9,9-dimethyl-9H-fluoren-2-yl)-N-(9,9-diphenyl-9H-fluoren-2-yl)dibenzo[b,d]furan-1-amine

Nom du produit:N-(9,9-dimethyl-9H-fluoren-2-yl)-N-(9,9-diphenyl-9H-fluoren-2-yl)dibenzo[b,d]furan-1-amine

IUPAC Name:N-(9,9-dimethyl-9H-fluoren-2-yl)-N-(9,9-diphenyl-9H-fluoren-2-yl)-8-oxatricyclo[7.4.0.0²,⁷]trideca-1(9),2,4,6,10,12-hexaen-3-amine

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: N° CAS:2356086-93-4; Formule moléculaire:C52H37NO; Point de fusion:-; Code SMILES:O1C=2C=CC=CC2C=3C1=CC=CC3N(C4=CC=C5C=6C=CC=CC6C(C=7C=CC=CC7)(C=8C=CC=CC8)C5=C4)C9=CC=C%10C=%11C=CC=CC%11C(C%10=C9)(C)C; Densité:

: Numéro de catalogue:CM1049329; Poids moléculaire:691.87; Point d'ébullition:; N° Mdl:; Stockage:

: Dibenzofurans; Dibenzofuran is an organic compound (C12H8O) consisting of two benzene rings fused to a central furan ring. Dibenzofuran can be synthesized by annealing and oxidative coupling methods of diphenyl ether, biphenyl derivatives, benzofuran, quinone. Most of the dibenzofuran-related natural products are metabolites of lichens or higher fungi. Lichen dibenzofurans appear to be formed by carbon-carbon oxidative coupling of orsellinic acid and its homologs.