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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-Ethoxy-2-formylphenylboronic acid

CCOc1ccc(c(c1)B(O)O)C=O Request for Quotation
Chemical Name: 5-Ethoxy-2-formylphenylboronic acid
CAS Number: 1003042-89-4
Product Number: AG0001JO(AGN-PC-0WABD7)
Synonyms:
MDL No:
Molecular Formula: C9H11BO4
Molecular Weight: 193.9922

Identification/Properties

Computed Properties
Molecular Weight:
193.993g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
4
Exact Mass:
194.075g/mol
Monoisotopic Mass:
194.075g/mol
Topological Polar Surface Area:
66.8A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
186
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


The (5-Ethoxy-2-formylphenyl)boronic acid is a versatile compound widely used in chemical synthesis. In organic chemistry, this boronic acid derivative serves as a valuable building block for the construction of diverse molecular structures. Its unique combination of functional groups, including the formyl and boronic acid moieties, enables selective reactions and efficient transformations in synthetic processes. One of the key applications of (5-Ethoxy-2-formylphenyl)boronic acid is in transition metal-catalyzed cross-coupling reactions, such as Suzuki-Miyaura coupling. By exploiting the boronic acid functionality, this compound can participate in palladium-catalyzed coupling reactions with aryl halides or pseudohalides, leading to the formation of biaryl compounds. The ethoxy and formyl groups further enhance the reactivity and selectivity of these transformations, allowing for the synthesis of complex molecules with high efficiency.Additionally, (5-Ethoxy-2-formylphenyl)boronic acid can be utilized in the selective functionalization of aromatic systems through C-H activation processes. The presence of the formyl group enables direct transformations at the ortho position of the phenyl ring, providing access to substituted arenes with precise regioselectivity. This reactivity profile makes (5-Ethoxy-2-formylphenyl)boronic acid a valuable tool for the elaboration of functionalized aromatic compounds in various chemical contexts.Overall, the (5-Ethoxy-2-formylphenyl)boronic acid represents a valuable reagent in modern organic synthesis, offering unique reactivity patterns and synthetic opportunities for the construction of complex molecular architectures. Its versatility and compatibility with diverse reaction conditions make it a valuable asset for chemists working in the field of organic chemistry.