1. Home
  2. (2-bromo-5-methoxypyridin-4-yl)boronic acid

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)-

(2-bromo-5-methoxypyridin-4-yl)boronic acid

COc1cnc(cc1B(O)O)Br Request for Quotation
Chemical Name: (2-bromo-5-methoxypyridin-4-yl)boronic acid
CAS Number: 1072952-48-7
Product Number: AG003BLV(AGN-PC-07138T)
Synonyms:
MDL No:
Molecular Formula: C6H7BBrNO3
Molecular Weight: 231.8397

Identification/Properties

Properties
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
231.84g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
2
Exact Mass:
230.97g/mol
Monoisotopic Mass:
230.97g/mol
Topological Polar Surface Area:
62.6A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
149
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

NMR Spectrum

Other Analytical Data

Request for Quotation

Customer Feedback

Chemical Structure


(2-Bromo-5-methoxypyridin-4-yl)boronic acid is a versatile compound commonly used in chemical synthesis as a valuable building block in the creation of various pharmaceuticals, agrochemicals, and materials. This boronic acid derivative serves as a key component in Suzuki-Miyaura cross-coupling reactions, a widely-used method for forming carbon-carbon bonds in organic synthesis.In organic chemistry, the Suzuki-Miyaura cross-coupling reaction involving (2-Bromo-5-methoxypyridin-4-yl)boronic acid allows for the selective and efficient assembly of complex molecular structures. By reacting this boronic acid derivative with suitable coupling partners under mild conditions catalyzed by palladium, chemists can link diverse functional groups together to create new chemical entities. This reaction has been instrumental in the development of numerous pharmaceuticals, including anti-cancer agents, antiviral drugs, and other bioactive molecules.Furthermore, the use of (2-Bromo-5-methoxypyridin-4-yl)boronic acid in chemical synthesis extends beyond the realm of medicinal chemistry. It finds application in the preparation of functional materials, such as molecular sensors, organic electronic components, and advanced polymers. By incorporating this boronic acid derivative into the molecular design, researchers can tailor the properties of the resulting materials, leading to enhanced performance characteristics and novel applications in various industries.Overall, the versatile nature of (2-Bromo-5-methoxypyridin-4-yl)boronic acid makes it an indispensable tool for chemists engaged in the synthesis of complex molecules and materials with tailored functionalities. Its role in facilitating Suzuki-Miyaura cross-coupling reactions highlights its significance as a key reagent in modern organic synthesis strategies.