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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)-

1,3,2-Dioxaborolane, 2-(4-fluorophenyl)-4,4,5,5-tetramethyl-

CC1(C)OB(OC1(C)C)c1ccc(cc1)F Request for Quotation
Chemical Name: 1,3,2-Dioxaborolane, 2-(4-fluorophenyl)-4,4,5,5-tetramethyl-
CAS Number: 214360-58-4
Product Number: AG0038W5(AGN-PC-0KKO1Z)
Synonyms:
MDL No:
Molecular Formula: C12H16BFO2
Molecular Weight: 222.0636

Identification/Properties

Computed Properties
Molecular Weight:
222.066g/mol
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
1
Exact Mass:
222.123g/mol
Monoisotopic Mass:
222.123g/mol
Topological Polar Surface Area:
18.5A^2
Heavy Atom Count:
16
Formal Charge:
0
Complexity:
244
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


2-(4-Fluorophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane, also known as $name$, is a versatile chemical compound widely utilized in chemical synthesis. This compound serves as a valuable building block in organic chemistry due to its unique properties and reactivity.One of the key applications of $name$ in chemical synthesis is its role as a boron-containing reagent in various cross-coupling reactions. For example, $name$ can be used in Suzuki-Miyaura cross-coupling reactions to facilitate the formation of carbon-carbon bonds. In this process, $name$ acts as a boron source, reacting with an aryl halide or pseudohalide in the presence of a palladium catalyst to yield biaryl compounds. This reaction is essential in the synthesis of pharmaceuticals, agrochemicals, and materials science.Additionally, $name$ can participate in other types of cross-coupling reactions such as Negishi and Hiyama coupling, offering a versatile tool for the creation of complex organic molecules. Its ability to undergo selective and efficient transformations makes it a valuable resource for synthetic chemists seeking to construct intricate molecular structures.Overall, the unique reactivity and versatility of 2-(4-Fluorophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane make it an indispensable component in the toolkit of organic chemists engaged in the synthesis of novel compounds with diverse applications.