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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, (3-methoxy-2-naphthalenyl)-

COc1cc2ccccc2cc1B(O)O Request for Quotation
Chemical Name: Boronic acid, (3-methoxy-2-naphthalenyl)-
CAS Number: 104115-76-6
Product Number: AG003894(AGN-PC-0NCAP2)
Synonyms:
MDL No:
Molecular Formula: C11H11BO3
Molecular Weight: 202.0142

Identification/Properties

Computed Properties
Molecular Weight:
202.016g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
2
Exact Mass:
202.08g/mol
Monoisotopic Mass:
202.08g/mol
Topological Polar Surface Area:
49.7A^2
Heavy Atom Count:
15
Formal Charge:
0
Complexity:
210
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#:
-
Hazard Statements:
H302
Precautionary Statements:
P280-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


3-Methoxy-2-naphthylboronic acid is a versatile compound widely utilized in chemical synthesis for its valuable properties. As a boronic acid derivative, it serves as a key building block in the synthesis of various organic molecules through Suzuki-Miyaura cross-coupling reactions. This compound acts as a crucial partner in forming carbon-carbon bonds, enabling the construction of complex molecular structures with high yields and efficiency. In particular, 3-Methoxy-2-naphthylboronic acid plays a significant role in the pharmaceutical industry, where it is employed in the development of novel drug candidates and research compounds. Its compatibility with a range of functional groups and reaction conditions makes it a valuable tool for organic chemists seeking to access diverse chemical space and create customized molecules for various applications. By using 3-Methoxy-2-naphthylboronic acid as a strategic building block, researchers can expedite the synthesis process and achieve precise control over the structural properties of the target compounds, paving the way for advancements in drug discovery, material science, and other areas of chemical research.