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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)-

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

CCOc1ncc(c(c1)B(O)O)Br Request for Quotation
Chemical Name: (5-bromo-2-ethoxypyridin-4-yl)boronic acid
CAS Number: 612845-46-2
Product Number: AG003BXO(AGN-PC-007075)
Synonyms:
MDL No:
Molecular Formula: C7H9BBrNO3
Molecular Weight: 245.8663

Identification/Properties

Properties
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
245.867g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
3
Exact Mass:
244.986g/mol
Monoisotopic Mass:
244.986g/mol
Topological Polar Surface Area:
62.6A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
161
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


Application:(5-Bromo-2-ethoxypyridin-4-yl)boronic acid is a versatile chemical compound widely used in organic synthesis as a key building block in the creation of complex molecules. This boronic acid derivative serves as an essential reagent in Suzuki-Miyaura cross-coupling reactions, a powerful tool in modern synthetic chemistry for forming carbon-carbon bonds. The unique properties of this compound make it particularly valuable in the synthesis of pharmaceuticals, agrochemicals, and materials science. Its ability to undergo efficient coupling reactions with various aryl halides and vinyl halides makes it a valuable tool for the installation of the pyridyl ether moiety in target molecules. Additionally, (5-Bromo-2-ethoxypyridin-4-yl)boronic acid can be utilized in the development of novel functional materials, such as ligands for catalysis and luminescent materials for applications in electronics and optoelectronics. This compound's broad applicability and compatibility with different reaction conditions highlight its significance in advancing the field of organic chemistry and enabling the synthesis of intricate molecular structures.