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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)-

Boronic acid, (5-methoxy-3-pyridinyl)-

COc1cncc(c1)B(O)O Request for Quotation
Chemical Name: Boronic acid, (5-methoxy-3-pyridinyl)-
CAS Number: 850991-69-4
Product Number: AG0036E5(AGN-PC-07H802)
Synonyms:
MDL No:
Molecular Formula: C6H8BNO3
Molecular Weight: 152.9436

Identification/Properties

Properties
BP:
356.2°C at 760 mmHg
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
152.944g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
2
Exact Mass:
153.06g/mol
Monoisotopic Mass:
153.06g/mol
Topological Polar Surface Area:
62.6A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
122
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
Precautionary Statements:
P264-P280-P302+P352+P332+P313+P362+P364-P305+P351+P338+P337+P313
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


5-Methoxypyridine-3-boronic acid is a versatile chemical compound widely used in organic synthesis as a building block to create various functional molecules. Its unique boronic acid group allows for selective cross-coupling reactions with other organic molecules, making it a valuable tool in the field of medicinal chemistry, agrochemicals, and material science.One of the key applications of 5-Methoxypyridine-3-boronic acid is in the Suzuki-Miyaura coupling reaction, where it serves as a boronate ester partner to form carbon-carbon bonds with aryl or vinyl halides under mild reaction conditions. This method enables the synthesis of complex organic compounds, such as pharmaceutical intermediates, natural product derivatives, and advanced materials.Additionally, 5-Methoxypyridine-3-boronic acid can be used to introduce the pyridine moiety into various molecular frameworks, imparting unique physicochemical properties to the final products. Its compatibility with a wide range of functional groups and ability to undergo diverse chemical transformations make it a valuable reagent for designing novel organic molecules with tailored properties for specific applications.