cas 2067322-25-0|| where to buy 4,6-Bis((S)-4-(tert-butyl)-4,5-dihydrooxazol-2-yl)dibenzo[b,d]furan

Nombre del producto:4,6-Bis((S)-4-(tert-butyl)-4,5-dihydrooxazol-2-yl)dibenzo[b,d]furan

IUPAC Name:(4S)-4-tert-butyl-2-{10-[(4S)-4-tert-butyl-4,5-dihydro-1,3-oxazol-2-yl]-8-oxatricyclo[7.4.0.0²,⁷]trideca-1(9),2(7),3,5,10,12-hexaen-6-yl}-4,5-dihydro-1,3-oxazole

: CAS：2067322-25-0; Fórmula molecular：C26H30N2O3; Pureza：95%+

: Número de catálogo：CM875155; Peso molecular：418.54

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: Núm. De CAS :2067322-25-0; Fórmula molecular:C26H30N2O3; Punto de fusión:-; Código de sonrisas:CC(C)(C)[C@H]1COC(=N1)C1=CC=CC2=C1OC1=C2C=CC=C1C1=N[C@H](CO1)C(C)(C)C; Densidad:

: Número de catálogo:CM875155; Peso molecular:418.54; Punto de ebullición:; Nº Mdl:; Almacenamiento:

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: Oxazolines; Oxazolines are five-membered heterocyclic compounds with one double bond. The double bond may be in one of three positions, so there may be three different oxazoline rings. The 2-oxazoline structure is the most common, and 3-oxazoline and 4-oxazoline exist mainly as laboratory research compounds. Oxazolines exist between oxazole and oxazolidine in terms of saturation.

: 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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