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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-fluoro-5-(morpholine-4-carbonyl)phenyl]boronic acid

O=C(c1ccc(c(c1)B(O)O)F)N1CCOCC1 Request for Quotation
Chemical Name: [2-fluoro-5-(morpholine-4-carbonyl)phenyl]boronic acid
CAS Number: 1072951-41-7
Product Number: AG003BN4(AGN-PC-07XU07)
Synonyms:
MDL No:
Molecular Formula: C11H13BFNO4
Molecular Weight: 253.0346

Identification/Properties

Properties
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
253.036g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
2
Exact Mass:
253.092g/mol
Monoisotopic Mass:
253.092g/mol
Topological Polar Surface Area:
70A^2
Heavy Atom Count:
18
Formal Charge:
0
Complexity:
299
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 boronic acid derivative (2-Fluoro-5-(morpholine-4-carbonyl)phenyl)boronic acid is a versatile compound widely employed in chemical synthesis as a key building block for the construction of complex organic molecules. Its unique structure, featuring a fluoro-substituted phenyl ring attached to a boronic acid moiety, imparts specific reactivity and functionality that make it valuable in various synthetic transformations.One of the primary applications of this compound is in the field of medicinal chemistry, where it serves as a crucial intermediate for the synthesis of bioactive molecules and pharmaceuticals. The presence of the boronic acid functional group enables the compound to participate in Suzuki-Miyaura cross-coupling reactions, facilitating the formation of carbon-carbon bonds and enabling the rapid assembly of structurally diverse compounds.Furthermore, the fluoro substituent on the phenyl ring can impart unique properties to the final products, such as improved pharmacokinetic profiles or enhanced biological activity. The morpholine-4-carbonyl group, on the other hand, can provide solubility enhancements or specific binding interactions with biological targets.Overall, the versatility and reactivity of (2-Fluoro-5-(morpholine-4-carbonyl)phenyl)boronic acid make it a valuable tool in the hands of synthetic chemists, enabling the efficient synthesis of novel organic molecules with potential applications in drug discovery, materials science, and other chemical fields.