2-dibenzofuran-4-yl-4,4,5,5-tetramethyl-1,3,2-dioxaborolane


Chemical Name: 2-dibenzofuran-4-yl-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
CAS Number: 912824-85-2
Product Number: AG00H2QG(AGN-PC-0DACWW)
Synonyms:
MDL No:
Molecular Formula: C18H19BO3
Molecular Weight: 294.1527

Identification/Properties


Computed Properties
Molecular Weight:
294.157g/mol
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
1
Exact Mass:
294.143g/mol
Monoisotopic Mass:
294.143g/mol
Topological Polar Surface Area:
31.6A^2
Heavy Atom Count:
22
Formal Charge:
0
Complexity:
420
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

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NMR Spectrum


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Chemical Structure



2-(Dibenzo[b,d]furan-4-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane is a versatile compound widely used in chemical synthesis. This boronic ester derivative plays a crucial role as a key building block in the field of organic chemistry. Its unique structure containing a dibenzofuran moiety provides enhanced reactivity and selectivity in various reactions.In chemical synthesis, 2-(Dibenzo[b,d]furan-4-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane is commonly employed as a boron reagent for Suzuki-Miyaura cross-coupling reactions. This powerful tool enables the efficient formation of carbon-carbon bonds, crucial for the construction of complex organic molecules. The presence of the boronic ester group facilitates the coupling process and allows for the incorporation of the dibenzofuran unit into the final product.Furthermore, this compound has demonstrated utility in the development of pharmaceuticals, agrochemicals, and materials science. Its strategic placement within molecular structures imparts beneficial properties and functionalities to the end products. By harnessing the chemical reactivity of 2-(Dibenzo[b,d]furan-4-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane, researchers can access a wide array of valuable derivatives with diverse applications.Overall, the significance of this boronic ester derivative lies in its ability to serve as a valuable synthetic tool for the creation of novel compounds with tailored properties. Its incorporation in chemical reactions broadens the scope of possibilities in organic synthesis and contributes to the advancement of scientific research and innovation.