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  2. 3-Fluoro-2-(4-Morpholino)pyridine-4-boronic acid pinacol ester

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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-2-(4-Morpholino)pyridine-4-boronic acid pinacol ester

Fc1c(nccc1B1OC(C(O1)(C)C)(C)C)N1CCOCC1 Request for Quotation
Chemical Name: 3-Fluoro-2-(4-Morpholino)pyridine-4-boronic acid pinacol ester
CAS Number: 957198-29-7
Product Number: AG003JF0(AGN-PC-0W5C8K)
Synonyms:
MDL No:
Molecular Formula: C15H22BFN2O3
Molecular Weight: 308.1562

Identification/Properties

Properties
Storage:
-10 ℃;
Form:
Solid
Computed Properties
Molecular Weight:
308.16g/mol
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
6
Rotatable Bond Count:
2
Exact Mass:
308.171g/mol
Monoisotopic Mass:
308.171g/mol
Topological Polar Surface Area:
43.8A^2
Heavy Atom Count:
22
Formal Charge:
0
Complexity:
388
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


4-(3-Fluoro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridin-2-yl)morpholine is a highly versatile compound used in chemical synthesis for the modification of organic molecules through cross-coupling reactions. This specific molecule serves as a valuable building block in the creation of complex organic structures due to its unique combination of functional groups.In organic synthesis, this compound can be employed in palladium-catalyzed cross-coupling reactions to introduce the 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridin-2-yl group onto various substrates. The fluorine atom at the 3-position further enhances the reactivity and selectivity of the molecule in these synthetic transformations.Additionally, the morpholine moiety of this compound can act as a versatile directing group in C-H activation reactions, enabling the regioselective functionalization of specific carbon-hydrogen bonds in target molecules. This feature is particularly useful for the late-stage modification of complex molecules in drug discovery and materials science research.Overall, 4-(3-Fluoro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridin-2-yl)morpholine plays a crucial role in modern chemical synthesis by providing chemists with a powerful tool for the controlled diversification of organic compounds, ultimately enabling the efficient construction of novel molecular architectures for various applications.