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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)-

(3-hydroxy-4-methylphenyl)boronic acid

OB(c1ccc(c(c1)O)C)O Request for Quotation
Chemical Name: (3-hydroxy-4-methylphenyl)boronic acid
CAS Number: 216019-35-1
Product Number: AG00BG3F(AGN-PC-0L6VEW)
Synonyms:
MDL No:
Molecular Formula: C7H9BO3
Molecular Weight: 151.9556

Identification/Properties

Computed Properties
Molecular Weight:
151.956g/mol
Hydrogen Bond Donor Count:
3
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
1
Exact Mass:
152.064g/mol
Monoisotopic Mass:
152.064g/mol
Topological Polar Surface Area:
60.7A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
129
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


3-Hydroxy-4-methylbenzeneboronic acid, also known as 3-Hydroxy-4-methylphenylboronic acid, is a versatile organic compound widely used in chemical synthesis. This compound is valued for its ability to act as a key building block in the preparation of various important organic molecules.One of the primary applications of 3-Hydroxy-4-methylbenzeneboronic acid is in the synthesis of pharmaceuticals. It serves as a crucial intermediate in the production of biologically active compounds, including potential pharmaceutical agents. By undergoing various reactions and functional group transformations, this compound can be used to create complex chemical structures needed for drug development.Furthermore, 3-Hydroxy-4-methylbenzeneboronic acid plays a significant role in the field of materials science. It is employed in the design and fabrication of advanced materials, such as polymers, liquid crystals, and optoelectronic components. The unique reactivity and properties of this compound enable researchers to tailor the characteristics of materials for specific applications, ranging from coatings to electronic devices.In addition to its applications in pharmaceutical and materials science, 3-Hydroxy-4-methylbenzeneboronic acid is utilized in the synthesis of agrochemicals, fragrances, and dyes. Its versatility and compatibility with various reaction conditions make it a valuable tool for chemists seeking to access diverse chemical functionalities and molecular structures.Overall, 3-Hydroxy-4-methylbenzeneboronic acid is a versatile and valuable compound in chemical synthesis, playing a crucial role in the creation of pharmaceuticals, materials, and specialty chemicals. Its widespread applicability and synthetic utility make it an essential component in the toolkit of organic chemists and researchers across different industries.