cas 1252914-65-0|| where to buy N1,N6-Diphenyl-N1,N6-bis(6-phenyl-4-dibenzofuranyl)-1,6-pyrenediamine

Produktname:N1,N6-Diphenyl-N1,N6-bis(6-phenyl-4-dibenzofuranyl)-1,6-pyrenediamine

IUPAC Name:N1,N6-diphenyl-N1,N6-bis({10-phenyl-8-oxatricyclo[7.4.0.0²,⁷]trideca-1(13),2,4,6,9,11-hexaen-6-yl})pyrene-1,6-diamine

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CM1049272-100mg	in stock	ǊǧŴ
CM1049272-250mg	in stock	ȬǊŴ
CM1049272-1g	in stock	ǧȁǊ

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: CAS-Nr.:1252914-65-0; Molekulare Formel:C64H40N2O2; Schmelzpunkt:-; SMILES-Code:C1(N(C2=CC=CC=C2)C3=C4OC5=C(C6=CC=CC=C6)C=CC=C5C4=CC=C3)=C(C7=C89)C=CC9=CC=C(N(C%10=CC=CC=C%10)C%11=C%12OC%13=C(C%14=CC=CC=C%14)C=CC=C%13C%12=CC=C%11)C8=CC=C7C=C1; Dichte:

: Katalognummer:CM1049272; Molekulargewicht:869.04; Siedepunkt:; Mdl-Nr.:; Lagerung:

: 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.