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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, (6-methoxy-2-naphthalenyl)-

COc1ccc2c(c1)ccc(c2)B(O)O Request for Quotation
Chemical Name: Boronic acid, (6-methoxy-2-naphthalenyl)-
CAS Number: 156641-98-4
Product Number: AG001OV2(AGN-PC-0LEOG6)
Synonyms:
MDL No: MFCD03093087
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


(6-Methoxynaphthalen-2-yl)boronic acid, also known as $name$, is a versatile compound widely used in chemical synthesis. As a boronic acid derivative, this compound plays a crucial role in Suzuki-Miyaura cross-coupling reactions, where it serves as a key component for creating carbon-carbon bonds. Its ability to react with various electrophiles, such as aryl halides and pseudohalides, makes it a valuable tool in the construction of complex organic molecules.Moreover, (6-Methoxynaphthalen-2-yl)boronic acid is particularly useful in the pharmaceutical industry for the synthesis of biologically active compounds and drug molecules. Its presence in drug development processes allows for the modification of molecular structures to enhance properties like bioavailability and potency. By forming stable boronate esters with reactive electrophiles, this compound facilitates the efficient creation of diverse chemical entities with potential therapeutic applications.Additionally, the unique structural features of (6-Methoxynaphthalen-2-yl)boronic acid make it a suitable building block for creating functional materials, such as organic light-emitting diodes (OLEDs) and organic semiconductors. Its compatibility with various synthetic procedures and its ability to undergo diverse transformations make it a valuable asset in the design and synthesis of advanced materials for electronic and optoelectronic devices.