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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)-

(4-ethoxy-3-methoxyphenyl)boronic acid

CCOc1ccc(cc1OC)B(O)O Request for Quotation
Chemical Name: (4-ethoxy-3-methoxyphenyl)boronic acid
CAS Number: 1189126-30-4
Product Number: AG007R97(AGN-PC-0AC0Z9)
Synonyms:
MDL No:
Molecular Formula: C9H13BO4
Molecular Weight: 196.0081

Identification/Properties

Computed Properties
Molecular Weight:
196.009g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
4
Exact Mass:
196.091g/mol
Monoisotopic Mass:
196.091g/mol
Topological Polar Surface Area:
58.9A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
165
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


The (4-Ethoxy-3-methoxyphenyl)boronic acid is a versatile compound widely used in chemical synthesis for its unique properties. As a boronic acid derivative, it serves as a crucial building block in organic chemistry, particularly in the field of Suzuki-Miyaura cross-coupling reactions. This compound plays a vital role in the formation of carbon-carbon bonds, making it an essential reagent for the synthesis of various organic molecules and pharmaceuticals. Additionally, (4-Ethoxy-3-methoxyphenyl)boronic acid exhibits excellent stability and compatibility with a wide range of functional groups, making it a valuable tool for the development of new materials and bioactive compounds in research and industrial applications.