cas 670258-91-0|| where to buy 8-oxatricyclo[7.4.0.0^{2,7}]trideca-1(9),2,4,6,10,12-hexaen-4-yl 3-oxo-2-azatricyclo[6.3.1.0^{4,12}]dodeca-1(12),4,6,8,10-pentaene-9-sulfonate

Product Name:8-oxatricyclo[7.4.0.0^{2,7}]trideca-1(9),2,4,6,10,12-hexaen-4-yl 3-oxo-2-azatricyclo[6.3.1.0^{4,12}]dodeca-1(12),4,6,8,10-pentaene-9-sulfonate

IUPAC Name:8-oxatricyclo[7.4.0.0²,⁷]trideca-1(9),2,4,6,10,12-hexaen-4-yl 3-oxo-2-azatricyclo[6.3.1.0⁴,¹²]dodeca-1(12),4,6,8,10-pentaene-9-sulfonate

: CAS：670258-91-0; Molecular Formula：C23H13NO5S; Purity：95%+

: Catalog Number：CM911599; Molecular Weight：415.42

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: CAS NO:670258-91-0; Molecular Formula:C23H13NO5S; Melting Point:-; Smiles Code:O=C1NC2=C3C1=CC=CC3=C(C=C2)S(=O)(=O)OC1=CC=C2OC3=C(C=CC=C3)C2=C1; Density:

: Catalog Number:CM911599; Molecular Weight:415.42; Boiling Point:; MDL No:; Storage:

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: 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.

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