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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, (4-ethoxyphenyl)-

CCOc1ccc(cc1)B(O)O Request for Quotation
Chemical Name: Boronic acid, (4-ethoxyphenyl)-
CAS Number: 22237-13-4
Product Number: AG003LBJ(AGN-PC-07HAG7)
Synonyms:
MDL No: MFCD00674028
Molecular Formula: C8H11BO3
Molecular Weight: 165.9821

Identification/Properties

Properties
MP:
121-128 °C(lit.)
BP:
317.6°C at 760 mmHg
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
165.983g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
3
Exact Mass:
166.08g/mol
Monoisotopic Mass:
166.08g/mol
Topological Polar Surface Area:
49.7A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
122
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


4-Ethoxyphenylboronic acid, also known as ethyl 4-boronoxybenzene, is a versatile compound commonly used in chemical synthesis. This compound plays a crucial role as a building block in the synthesis of various pharmaceuticals and agrochemicals. It is particularly valued for its ability to act as a boronic acid derivative, which enables it to participate in numerous cross-coupling reactions, such as the Suzuki-Miyaura coupling reaction.In chemical synthesis, 4-Ethoxyphenylboronic acid serves as a key intermediate in the production of biologically active compounds, including drug candidates and insecticides. By reacting with various electrophiles under suitable conditions, this compound allows for the formation of complex molecular structures with high efficiency and selectivity. Its compatibility with a wide range of functional groups makes it a valuable tool for the construction of intricate organic molecules.Furthermore, the unique properties of 4-Ethoxyphenylboronic acid make it an essential component in the development of innovative materials and catalysts. Its ability to participate in carbon-carbon bond formation reactions makes it a crucial element in the design and synthesis of advanced organic materials with tailored properties.Overall, 4-Ethoxyphenylboronic acid is a versatile and indispensable compound in chemical synthesis, offering a wide range of applications in the creation of diverse chemical products with pharmaceutical, agricultural, and materials science significance.