Nombre del producto:2-Chloro-4-(dibenzo[b,d]furan-3-yl)-6-(naphthalen-2-yl)-1,3,5-triazine

IUPAC Name:2-chloro-4-(naphthalen-2-yl)-6-{8-oxatricyclo[7.4.0.0²,⁷]trideca-1(13),2,4,6,9,11-hexaen-5-yl}-1,3,5-triazine

CAS:2226747-69-7
Fórmula molecular:C25H14ClN3O
Pureza:95%+
Número de catálogo:CM558849
Peso molecular:407.86

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CM558849-25g in stock ɅŴȷȷ

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Detalles del producto

Núm. De CAS :2226747-69-7
Fórmula molecular:C25H14ClN3O
Punto de fusión:-
Código de sonrisas:ClC1=NC(C2=CC=C3C(OC4=CC=CC=C34)=C2)=NC(C5=CC=C6C=CC=CC6=C5)=N1
Densidad:
Número de catálogo:CM558849
Peso molecular:407.86
Punto de ebullición:
Nº Mdl:
Almacenamiento:

Category Infos

Naphthalenes
Naphthalene is a hydrocarbon produced by the distillation of coal tar and is an aromatic white crystalline substance. Naphthalene is the most abundant component in coal tar. It is used as an insect repellant and insect fumigant. The compound is used in the manufacture of celluloid, dyes, hydrogenated naphthalenes, oil fumes, smokeless powders and synthetic resins.
Triazines
Triazines are an important class of six-membered aromatic heterocycles with three nitrogen atoms that give rise to three regioisomers: 1,2,4-triazines, 1,2,3-triazines, and 1,3, 5-triazine. 1,2,3-Triazines show remarkable reactivity and have attracted attention for their medicinal value. Triazine compounds fused with other carbon and heterocycles are stable and have a broad spectrum of pharmacological activities.
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.