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  2. 2-(2,3-dihydro-1-benzofuran-7-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

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Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-
O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]
Tris(dibenzylideneacetone)dipalladium
C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C
Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

2-(2,3-dihydro-1-benzofuran-7-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

CC1(C)OB(OC1(C)C)c1cccc2c1OCC2 Request for Quotation
Chemical Name: 2-(2,3-dihydro-1-benzofuran-7-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
CAS Number: 934586-50-2
Product Number: AG0039R3(AGN-PC-06V8IB)
Synonyms:
MDL No:
Molecular Formula: C14H19BO3
Molecular Weight: 246.1099

Identification/Properties

Computed Properties
Molecular Weight:
246.113g/mol
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
1
Exact Mass:
246.143g/mol
Monoisotopic Mass:
246.143g/mol
Topological Polar Surface Area:
27.7A^2
Heavy Atom Count:
18
Formal Charge:
0
Complexity:
313
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

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
-
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P280-P301+P312-P302+P352-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


The application of 2-(2,3-Dihydrobenzofuran-7-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane in chemical synthesis lies in its ability to serve as a valuable building block for the construction of complex organic molecules. This boron-containing compound is commonly used in Suzuki-Miyaura cross-coupling reactions, a versatile method in organic chemistry that allows for the formation of carbon-carbon bonds.By incorporating 2-(2,3-Dihydrobenzofuran-7-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane into the reaction, chemists can facilitate the coupling of this boron derivative with a variety of organic electrophiles, such as aryl halides or pseudohalides. This process enables the synthesis of biaryl compounds, which are fundamental structural motifs found in many pharmaceuticals, agrochemicals, and materials.Furthermore, the unique structural features of 2-(2,3-Dihydrobenzofuran-7-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane provide chemists with opportunities to access diverse chemical space and create molecular complexity efficiently. Its selective reactivity and compatibility with other functional groups make it a valuable tool for the construction of natural products, ligands, and fine chemicals in the field of organic synthesis.