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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, (3-formyl-4-methoxyphenyl)-

O=Cc1cc(ccc1OC)B(O)O Request for Quotation
Chemical Name: Boronic acid, (3-formyl-4-methoxyphenyl)-
CAS Number: 121124-97-8
Product Number: AG0037VV(AGN-PC-0KKN2O)
Synonyms:
MDL No: MFCD02093661
Molecular Formula: C8H9BO4
Molecular Weight: 179.9657

Identification/Properties

Computed Properties
Molecular Weight:
179.966g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
3
Exact Mass:
180.059g/mol
Monoisotopic Mass:
180.059g/mol
Topological Polar Surface Area:
66.8A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
174
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


3-Formyl-4-methoxyphenylboronic acid, also known as $name$, serves a crucial role in chemical synthesis as a versatile building block for the creation of various organic compounds. This compound has found significant utility in the field of medicinal chemistry, particularly in the design and development of pharmaceuticals.The aldehyde group present in $name$ can participate in numerous organic reactions, such as condensation reactions, to form new carbon-carbon bonds. Additionally, the boronic acid moiety enables $name$ to undergo Suzuki-Miyaura cross-coupling reactions with aryl halides, providing a powerful tool for the synthesis of biaryl compounds.Furthermore, the methoxy substituent on the phenyl ring of $name$ can influence its reactivity and selectivity in chemical transformations, making it a valuable functional group for tailoring the properties of the final products. By utilizing the unique reactivity of each component in $name$, chemists can efficiently construct complex molecular structures with precise control over stereochemistry and functionality.