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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-methoxynaphthalen-1-yl)boronic acid

COc1cc(B(O)O)c2c(c1)cccc2 Request for Quotation
Chemical Name: (3-methoxynaphthalen-1-yl)boronic acid
CAS Number: 219834-94-3
Product Number: AG00385M(AGN-PC-03ZDTK)
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#:
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


The (3-Methoxynaphthalen-1-yl)boronic acid is a versatile chemical compound widely used in organic synthesis processes. This boronic acid derivative is particularly valuable as a key building block in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds under mild conditions. By serving as a boronate ester source, this compound facilitates the incorporation of the (3-Methoxynaphthalen-1-yl) functionality into complex molecules, thus allowing for the creation of diverse molecular architectures. Its compatibility with various functional groups and its ability to participate in selective transformations make it a valuable tool for the synthesis of pharmaceuticals, agrochemicals, and materials with tailored properties. Additionally, the (3-Methoxynaphthalen-1-yl)boronic acid's stability and ease of manipulation further enhance its utility in the preparation of novel compounds for research and industrial applications.