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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-(2-fluorophenyl)-4,4,5,5-tetramethyl-

Fc1ccccc1B1OC(C(O1)(C)C)(C)C Request for Quotation
Chemical Name: 1,3,2-Dioxaborolane, 2-(2-fluorophenyl)-4,4,5,5-tetramethyl-
CAS Number: 876062-39-4
Product Number: AG0036BJ(AGN-PC-0NHZ0G)
Synonyms:
MDL No:
Molecular Formula: C12H16BFO2
Molecular Weight: 222.0636

Identification/Properties

Properties
BP:
284.6±23.0°C at 760 mmHg
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Refractive Index:
1.4830 to 1.4870
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:
252
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#:
N/A
Hazard Statements:
H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


The 2-Fluorophenylboronic acid, pinacol ester is a highly versatile compound widely used in chemical synthesis processes. This compound serves as a key building block in the creation of various pharmaceuticals, agrochemicals, and materials.Its unique structure enables it to participate in a range of reactions, such as Suzuki-Miyaura cross-coupling reactions, Buchwald-Hartwig amination, and Heck reactions. These reactions are essential in the synthesis of complex organic molecules and play a crucial role in drug discovery and development.Additionally, the 2-Fluorophenylboronic acid, pinacol ester can be employed in the modification of biomolecules, the functionalization of polymers, and the preparation of advanced materials with tailored properties. Its compatibility with other reagents and ability to undergo selective transformations make it a valuable tool for chemical researchers and synthetic chemists seeking to create novel molecules with specific functionalities.