Product Name:2-(Dibenzo[b,d]furan-4-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

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

CAS:912824-85-2
Molecular Formula:C18H19BO3
Purity:95%
Catalog Number:CM135565
Molecular Weight:294.16

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Product Details

CAS NO:912824-85-2
Molecular Formula:C18H19BO3
Melting Point:-
Smiles Code:CC1(C)C(C)(C)OB(C2=C3OC4=CC=CC=C4C3=CC=C2)O1
Density:
Catalog Number:CM135565
Molecular Weight:294.16
Boiling Point:
MDL No:MFCD18910632
Storage:

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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