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  2. 2-(5-bromo-2-fluorophenyl)-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-(5-bromo-2-fluorophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

CC1(C)OB(OC1(C)C)c1cc(Br)ccc1F Request for Quotation
Chemical Name: 2-(5-bromo-2-fluorophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
CAS Number: 942069-51-4
Product Number: AG005SN7(AGN-PC-0786KM)
Synonyms:
MDL No:
Molecular Formula: C12H15BBrFO2
Molecular Weight: 300.9597

Identification/Properties

Properties
Storage:
2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
300.962g/mol
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
1
Exact Mass:
300.033g/mol
Monoisotopic Mass:
300.033g/mol
Topological Polar Surface Area:
18.5A^2
Heavy Atom Count:
17
Formal Charge:
0
Complexity:
282
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:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


The 2-(5-Bromo-2-fluorophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane is a versatile chemical reagent commonly used in organic synthesis. Its unique structure containing boron and halogen atoms makes it a valuable building block in the preparation of various organic compounds. One key application of this compound is its use as a boron source in Suzuki-Miyaura cross-coupling reactions. In this reaction, the 2-(5-Bromo-2-fluorophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane reacts with an aryl or vinyl halide in the presence of a palladium catalyst to form a new carbon-carbon bond. This method is widely employed in the synthesis of pharmaceuticals, agrochemicals, and materials science.Additionally, this compound can also participate in other types of C-C bond-forming reactions such as Heck and Sonogashira reactions, providing chemists with a powerful tool for constructing complex organic molecules. Its stability and compatibility with a variety of functional groups make it a valuable asset in the toolbox of synthetic chemists.