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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, (2-ethoxy-3-pyridinyl)-

CCOc1ncccc1B(O)O Request for Quotation
Chemical Name: Boronic acid, (2-ethoxy-3-pyridinyl)-
CAS Number: 854373-97-0
Product Number: AG0038DY(AGN-PC-006I9P)
Synonyms:
MDL No: MFCD06201036
Molecular Formula: C7H10BNO3
Molecular Weight: 166.9702

Identification/Properties

Computed Properties
Molecular Weight:
166.971g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
3
Exact Mass:
167.075g/mol
Monoisotopic Mass:
167.075g/mol
Topological Polar Surface Area:
62.6A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
134
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

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Chemical Structure


2-Ethoxy-3-pyridineboronic acid is a vital reagent widely employed in chemical synthesis due to its unique properties and versatility. This compound serves as a key building block in the construction of various heterocyclic compounds and pharmaceutical molecules. Its ability to participate in Suzuki-Miyaura cross-coupling reactions makes it a valuable tool in the synthesis of biaryl compounds, which are prevalent in pharmaceuticals, agrochemicals, and materials science. Furthermore, 2-Ethoxy-3-pyridineboronic acid can be utilized in the functionalization of aromatic systems through palladium-catalyzed C-H activation, allowing for the selective introduction of desired substituents. Its strategic incorporation in organic synthesis enables the rapid and efficient assembly of complex molecular architectures with high precision and control.