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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)-

3-Fluoro-4-morpholinophenylboronic Acid

Fc1cc(ccc1N1CCOCC1)B(O)O Request for Quotation
Chemical Name: 3-Fluoro-4-morpholinophenylboronic Acid
CAS Number: 279262-09-8
Product Number: AG0033PC(AGN-PC-09SGGK)
Synonyms:
MDL No: MFCD16883060
Molecular Formula: C10H13BFNO3
Molecular Weight: 225.0245

Identification/Properties

Properties
BP:
420.416°C at 760 mmHg
Storage:
Inert atmosphere;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
225.026g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
2
Exact Mass:
225.097g/mol
Monoisotopic Mass:
225.097g/mol
Topological Polar Surface Area:
52.9A^2
Heavy Atom Count:
16
Formal Charge:
0
Complexity:
226
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


The (3-Fluoro-4-morpholinophenyl)boronic acid is a versatile compound widely used in chemical synthesis as a key building block in the preparation of pharmaceuticals and agrochemicals. This boronic acid derivative is particularly valuable in cross-coupling reactions with aryl halides or pseudohalides to form carbon-carbon bonds, a fundamental transformation in organic chemistry. Its unique combination of a fluorine atom and a morpholine group allows for selective incorporation of these functionalities into the target molecules, enhancing their biological activities or physical properties. Furthermore, the boronic acid moiety confers reactivity towards Suzuki-Miyaura coupling, enabling the rapid and efficient assembly of complex molecular structures. Additionally, the presence of the boronic acid group offers the potential for further derivatization, making this compound a valuable tool in the design and synthesis of innovative chemical entities with diverse applications in medicinal chemistry and materials science.