1. Home
  2. Boronicacid, B-[5-(methylsulfonyl)-3-pyridinyl]-

Contact Angene

Tel: +852 8191 6999

Email: [email protected]

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-[5-(methylsulfonyl)-3-pyridinyl]-

OB(c1cncc(c1)S(=O)(=O)C)O Request for Quotation
Chemical Name: Boronicacid, B-[5-(methylsulfonyl)-3-pyridinyl]-
CAS Number: 913836-01-8
Product Number: AG00GSYB(AGN-PC-07138R)
Synonyms:
MDL No: MFCD08689536
Molecular Formula: C6H8BNO4S
Molecular Weight: 201.0080

Identification/Properties

Properties
MP:
123-125°C
BP:
523.8°C at 760 mmHg
Storage:
2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
201.003g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
2
Exact Mass:
201.027g/mol
Monoisotopic Mass:
201.027g/mol
Topological Polar Surface Area:
95.9A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
260
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-H332-H335
Precautionary Statements:
P280-P305+P351+P338-P310
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

Request for Quotation

Customer Feedback

Chemical Structure


Known for its versatile applications in chemical synthesis, B-[5-(Methylsulfonyl)-3-pyridinyl]boronic acid serves as a crucial building block for the creation of advanced organic compounds. This compound uniquely combines the reactivity of boronic acids with the electron-donating properties of the pyridine ring, making it an indispensable tool in the toolbox of synthetic chemists.In the realm of chemical synthesis, B-[5-(Methylsulfonyl)-3-pyridinyl]boronic acid is frequently employed in Suzuki-Miyaura cross-coupling reactions, a cornerstone of modern organic synthesis. This reaction allows for the selective formation of carbon-carbon bonds under mild conditions, enabling the efficient assembly of complex molecular structures. By utilizing B-[5-(Methylsulfonyl)-3-pyridinyl]boronic acid as a key reactant in these transformations, chemists can access a wide array of functionalized molecules with tailored properties.Moreover, the presence of the methylsulfonyl group in B-[5-(Methylsulfonyl)-3-pyridinyl]boronic acid further enhances its utility in organic synthesis. This functional group not only provides structural diversity but also imparts unique chemical reactivity, enabling the selective modification of the pyridine ring and facilitating the construction of intricate molecular architectures.In summary, B-[5-(Methylsulfonyl)-3-pyridinyl]boronic acid stands as a valuable asset in the hands of synthetic chemists, offering a powerful platform for the construction of diverse organic compounds through strategic bond-forming reactions. Its versatility, reactivity, and structural features make it an indispensable component in the toolkit of those engaged in the art of chemical synthesis.