1. Home
  2. Boronic acid, [3-(2-naphthalenyl)phenyl]-

Contact Angene

Tel: +852 8191 6999

Email: [email protected]

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-(2-naphthalenyl)phenyl]-

OB(c1cccc(c1)c1ccc2c(c1)cccc2)O Request for Quotation
Chemical Name: Boronic acid, [3-(2-naphthalenyl)phenyl]-
CAS Number: 870774-29-1
Product Number: AG008DLD(AGN-PC-07CLYW)
Synonyms:
MDL No:
Molecular Formula: C16H13BO2
Molecular Weight: 248.0842

Identification/Properties

Computed Properties
Molecular Weight:
248.088g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
2
Exact Mass:
248.101g/mol
Monoisotopic Mass:
248.101g/mol
Topological Polar Surface Area:
40.5A^2
Heavy Atom Count:
19
Formal Charge:
0
Complexity:
295
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

Request for Quotation

Customer Feedback

Chemical Structure


(3-(Naphthalen-2-yl)phenyl)boronic acid is a versatile compound commonly used in chemical synthesis, particularly in the field of organic chemistry. This specific boronic acid derivative is valued for its ability to participate in Suzuki-Miyaura cross-coupling reactions, a popular method for forming carbon-carbon bonds.When employed in chemical synthesis, (3-(Naphthalen-2-yl)phenyl)boronic acid serves as a key component in creating complex organic molecules, pharmaceuticals, and materials. Its compatibility with various functional groups and its high reactivity make it an essential reagent for constructing intricate molecular structures.Furthermore, the incorporation of (3-(Naphthalen-2-yl)phenyl)boronic acid in synthetic procedures enables chemists to access a broad range of substituted aromatic compounds and heterocycles. Its straightforward usage and reliability in forging new bonds make it a valuable tool for researchers and industry professionals alike who are engaged in the synthesis of novel molecules with diverse applications.