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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, (6-methyl-3-pyridinyl)-

Cc1ccc(cn1)B(O)O Request for Quotation
Chemical Name: Boronic acid, (6-methyl-3-pyridinyl)-
CAS Number: 659742-21-9
Product Number: AG003HW5(AGN-PC-07H84V)
Synonyms:
MDL No: MFCD06801736
Molecular Formula: C6H8BNO2
Molecular Weight: 136.9442

Identification/Properties

Properties
MP:
128-130°C
Storage:
Inert atmosphere;-10 ℃;
Form:
Solid
Computed Properties
Molecular Weight:
136.945g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
1
Exact Mass:
137.065g/mol
Monoisotopic Mass:
137.065g/mol
Topological Polar Surface Area:
53.4A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
110
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-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


(6-Methylpyridin-3-yl)boronic acid, also known as 6-MePyB(OH)2, is a versatile compound widely used in chemical synthesis as a boronic acid derivative. It serves as a valuable building block in organic chemistry due to its ability to participate in various cross-coupling reactions, such as Suzuki-Miyaura and Heck reactions, which are essential in the formation of carbon-carbon bonds.One of the key applications of (6-Methylpyridin-3-yl)boronic acid is in the synthesis of pharmaceuticals, agrochemicals, and materials. Its unique structure and reactivity make it a valuable tool for introducing the 6-methylpyridin-3-yl group into target molecules, imparting specific properties or functions. This compound plays a crucial role in the development of new drugs, functional materials, and advanced organic compounds.Additionally, (6-Methylpyridin-3-yl)boronic acid is utilized in the preparation of ligands for catalysis and as a key intermediate in the synthesis of complex organic molecules. Its compatibility with various functional groups and reagents makes it a versatile and indispensable reagent in modern organic synthesis. By incorporating this boronic acid derivative into chemical reactions, researchers can achieve selective and efficient transformations, facilitating the construction of complex molecular structures.In summary, (6-Methylpyridin-3-yl)boronic acid is a valuable reagent with diverse applications in chemical synthesis, particularly in the creation of pharmaceuticals, agrochemicals, materials, and complex organic molecules. Its unique properties and reactivity allow for the efficient construction of novel compounds and the development of cutting-edge technologies in the field of organic chemistry.