Nombre del producto:Dibenzofuran-4-boronic acid

IUPAC Name:{8-oxatricyclo[7.4.0.0²,⁷]trideca-1(13),2,4,6,9,11-hexaen-6-yl}boronic acid

CAS:100124-06-9
Fórmula molecular:C12H9BO3
Pureza:98%
Número de catálogo:CM137540
Peso molecular:212.01

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CM137540-100g in stock NJʼnư
CM137540-500g in stock ŢĽNJ

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Detalles del producto

Núm. De CAS :100124-06-9
Fórmula molecular:C12H9BO3
Punto de fusión:-
Código de sonrisas:OB(C1=C2OC3=CC=CC=C3C2=CC=C1)O
Densidad:
Número de catálogo:CM137540
Peso molecular:212.01
Punto de ebullición:
Nº Mdl:MFCD00092336
Almacenamiento:

Category Infos

Boronic Acids and Esters
Boronic acids and boronate esters are commonly used reagents in Suzuki–Miyaura coupling chemistry. Organoboron derivatives are common reagents for C–C bond formation, either through classical palladium-mediated transformations or through other newer coupling methods. Boronic esters and acids are potential intermediates in the manufacture of many active pharmaceutical ingredients (API).
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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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