Название продукции: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
Молекулярная формула:C12H9BO3
Чистота:98%
Номер в каталоге:CM137540
Молекулярная масса:212.01

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Информация о продукции

Номер CAS:100124-06-9
Молекулярная формула:C12H9BO3
Точка плавления:-
Smiles-код:OB(C1=C2OC3=CC=CC=C3C2=CC=C1)O
Плотность:
Номер в каталоге:CM137540
Молекулярная масса:212.01
Точка кипения:
Номер Mdl:MFCD00092336
Хранение:

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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