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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-(methylthio)-3-pyridinyl]-

CSc1cncc(c1)B(O)O Request for Quotation
Chemical Name: Boronic acid, [5-(methylthio)-3-pyridinyl]-
CAS Number: 477251-98-2
Product Number: AG006ZQG(AGN-PC-03ON7T)
Synonyms:
MDL No:
Molecular Formula: C6H8BNO2S
Molecular Weight: 169.0092

Identification/Properties

Computed Properties
Molecular Weight:
169.005g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
2
Exact Mass:
169.037g/mol
Monoisotopic Mass:
169.037g/mol
Topological Polar Surface Area:
78.6A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
125
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:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


Containing the unique and versatile (5-(Methylthio)pyridin-3-yl)boronic acid, this product plays a crucial role in various chemical synthesis processes. Its importance lies in its ability to act as a valuable building block for creating a wide range of complex organic molecules. (5-(Methylthio)pyridin-3-yl)boronic acid is frequently utilized in Suzuki-Miyaura cross-coupling reactions, where it serves as a key component in forming carbon-carbon bonds. This compound has been found to exhibit excellent reactivity and selectivity in such reactions, making it a preferred choice for chemists working on the synthesis of biologically active compounds, pharmaceuticals, and advanced materials.Moreover, the presence of the boronic acid group in this compound allows for further functionalization through various chemical transformations, thereby enabling the synthesis of diverse molecular structures with tailored properties. Its versatility and compatibility with a wide range of reaction conditions make (5-(Methylthio)pyridin-3-yl)boronic acid a valuable tool for synthetic chemists striving to access new molecules for research and industrial applications.