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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Detalles del producto

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:

Category Infos

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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