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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)-

5-FLUORO-2-METHOXYPYRIDINE-3-BORONIC ACID

COc1ncc(cc1B(O)O)F Request for Quotation
Chemical Name: 5-FLUORO-2-METHOXYPYRIDINE-3-BORONIC ACID
CAS Number: 957120-32-0
Product Number: AG00H80X(AGN-PC-0786ML)
Synonyms:
MDL No:
Molecular Formula: C6H7BFNO3
Molecular Weight: 170.9341

Identification/Properties

Properties
BP:
327.6°C at 760 mmHg
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
170.934g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
2
Exact Mass:
171.05g/mol
Monoisotopic Mass:
171.05g/mol
Topological Polar Surface Area:
62.6A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
149
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#:
-
Hazard Statements:
H302
Precautionary Statements:
P280-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


The (5-Fluoro-2-methoxypyridin-3-yl)boronic acid is a versatile reagent commonly used in chemical synthesis due to its unique properties. It serves as a key building block in the development of pharmaceuticals, agrochemicals, and materials science. Its boronic acid functionality makes it particularly valuable in Suzuki-Miyaura cross-coupling reactions, where it can undergo oxidative addition with aryl or vinyl halides in the presence of a palladium catalyst. This reaction allows for the formation of carbon-carbon bonds, enabling the synthesis of complex organic compounds. Additionally, the fluoro and methoxy substituents on the pyridine ring can impart specific properties to the final molecule, such as improved solubility, bioavailability, or reactivity. The (5-Fluoro-2-methoxypyridin-3-yl)boronic acid thus plays a crucial role in the efficient and strategic construction of diverse chemical structures for various applications.