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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)-

(2-formyl-5-methylphenyl)boronic acid

O=Cc1ccc(cc1B(O)O)C Request for Quotation
Chemical Name: (2-formyl-5-methylphenyl)boronic acid
CAS Number: 40138-17-8
Product Number: AG003HCB(AGN-PC-0KZ6WL)
Synonyms:
MDL No:
Molecular Formula: C8H9BO3
Molecular Weight: 163.9663

Identification/Properties

Properties
BP:
375.3°C at 760 mmHg
Storage:
Inert atmosphere;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
163.967g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
2
Exact Mass:
164.064g/mol
Monoisotopic Mass:
164.064g/mol
Topological Polar Surface Area:
57.5A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
160
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-Formyl-5-methylphenylboronic acid, also known as $name$, plays a crucial role in chemical synthesis as a versatile building block in organic chemistry. Its unique structure containing both a formyl group and a boronic acid moiety makes it a valuable reagent with diverse applications.One of the key uses of $name$ in chemical synthesis is as a cross-coupling reagent in Suzuki-Miyaura reactions. By reacting with various aryl or vinyl halides in the presence of a palladium catalyst, 2-Formyl-5-methylphenylboronic acid can facilitate the formation of biaryl compounds and other complex organic molecules. This reaction is highly efficient and widely employed in the synthesis of pharmaceuticals, agrochemicals, and materials science.Moreover, $name$ can participate in direct functionalization reactions by forming carbon-carbon bonds through C-H activation processes. This capability allows for the selective modification of aromatic rings, enabling the design and synthesis of new molecules with tailored properties.In summary, 2-Formyl-5-methylphenylboronic acid is a versatile reagent that finds extensive use in organic synthesis for constructing complex molecular structures and enabling the development of novel chemical entities.