cas 1423035-06-6|| where to buy 2,2,2-Trifluoroethyl n-{4-methoxy-8-oxatricyclo[7.4.0.0,2,7]trideca-1(9),2(7),3,5,10,12-hexaen-5-yl}carbamate

Nombre del producto:2,2,2-Trifluoroethyl n-{4-methoxy-8-oxatricyclo[7.4.0.0,2,7]trideca-1(9),2(7),3,5,10,12-hexaen-5-yl}carbamate

IUPAC Name:2,2,2-trifluoroethyl N-{4-methoxy-8-oxatricyclo[7.4.0.0²,⁷]trideca-1(9),2(7),3,5,10,12-hexaen-5-yl}carbamate

Unidad de embalaje	Stock disponible	Precio($)
CM1049004-50mg	in stock	ȷǆǕ
CM1049004-100mg	in stock	ȌƋȷ
CM1049004-250mg	in stock	ɐȦƤ
CM1049004-500mg	in stock	ȦȦǲȷ
CM1049004-1g	in stock	ȦſƋƤ
CM1049004-5g	in stock	ȌȌɐȌ

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: Núm. De CAS :1423035-06-6; Fórmula molecular:C16H12F3NO4; Punto de fusión:-; Código de sonrisas:O=C(OCC(F)(F)F)NC1=CC2=C(C=C1OC)C3=C(C=CC=C3)O2; Densidad:

: Número de catálogo:CM1049004; Peso molecular:339.27; Punto de ebullición:390.5±42.0 °C at 760 mmHg; Nº Mdl:; Almacenamiento:

: 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.