Boronic acid, (4-methoxy-2,5-dimethylphenyl)-


Chemical Name: Boronic acid, (4-methoxy-2,5-dimethylphenyl)-
CAS Number: 246023-54-1
Product Number: AG002OQ9(AGN-PC-0LOWB1)
Synonyms:
MDL No:
Molecular Formula: C9H13BO3
Molecular Weight: 180.0087

Identification/Properties


Properties
BP:
340 °C at 760 mmHg
Storage:
2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
180.01g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
2
Exact Mass:
180.096g/mol
Monoisotopic Mass:
180.096g/mol
Topological Polar Surface Area:
49.7A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
163
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:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum


Other Analytical Data


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Chemical Structure



2,5-Dimethyl-4-methoxyphenylboronic acid is a versatile chemical compound widely used in organic synthesis, particularly in the field of medicinal chemistry and pharmaceuticals. This compound serves as a valuable building block in the synthesis of various biologically active molecules due to its unique structural properties and reactivity.One of the key applications of 2,5-Dimethyl-4-methoxyphenylboronic acid is its role as a key component in Suzuki-Miyaura cross-coupling reactions. This powerful synthetic method allows for the formation of carbon-carbon bonds under mild conditions, making it a valuable tool in the construction of complex organic molecules. By using 2,5-Dimethyl-4-methoxyphenylboronic acid as a coupling partner, chemists can efficiently introduce the phenylboronic acid motif into target molecules, enabling the rapid and efficient synthesis of diverse chemical compounds.Furthermore, 2,5-Dimethyl-4-methoxyphenylboronic acid can also be utilized as a directing group in transition metal-catalyzed C-H activation reactions. In this context, the boronic acid moiety can direct the selective functionalization of specific carbon-hydrogen bonds within complex molecules, leading to the regioselective synthesis of novel organic compounds with high efficiency and precision.Overall, the unique reactivity and versatility of 2,5-Dimethyl-4-methoxyphenylboronic acid make it an indispensable tool for chemists engaged in the synthesis of new pharmaceuticals, agrochemicals, and materials with tailored properties.