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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)-

Boronicacid, B-[6-(hydroxymethyl)-3-pyridinyl]-

OCc1ccc(cn1)B(O)O Request for Quotation
Chemical Name: Boronicacid, B-[6-(hydroxymethyl)-3-pyridinyl]-
CAS Number: 913835-98-0
Product Number: AG006BHO(AGN-PC-0712IE)
Synonyms:
MDL No: MFCD09027230
Molecular Formula: C6H8BNO3
Molecular Weight: 152.9436

Identification/Properties

Properties
BP:
384 °C at 760 mmHg
Storage:
2-8℃;
Computed Properties
Molecular Weight:
152.944g/mol
Hydrogen Bond Donor Count:
3
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
2
Exact Mass:
153.06g/mol
Monoisotopic Mass:
153.06g/mol
Topological Polar Surface Area:
73.6A^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#:
-
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


The (6-(Hydroxymethyl)pyridin-3-yl)boronic acid is a versatile compound widely utilized in chemical synthesis as a key building block in the formation of various organic molecules. Due to its boronic acid functionality, this compound is particularly valuable in Suzuki-Miyaura cross-coupling reactions, enabling the efficient construction of carbon-carbon bonds. By acting as a coupling partner with aryl halides or pseudohalides under palladium catalysis, (6-(Hydroxymethyl)pyridin-3-yl)boronic acid facilitates the creation of complex organic structures with high selectivity and efficiency. Its application extends to the synthesis of pharmaceuticals, agrochemicals, and materials where precise control over molecular architecture is essential. Furthermore, this compound's hydroxymethyl group provides additional chemical functionality for further derivatization and diversification, making it a valuable tool in the hands of synthetic chemists.