1. Home
  2. (4-naphthalen-2-ylphenyl)boronic acid

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)-

(4-naphthalen-2-ylphenyl)boronic acid

OB(c1ccc(cc1)c1ccc2c(c1)cccc2)O Request for Quotation
Chemical Name: (4-naphthalen-2-ylphenyl)boronic acid
CAS Number: 918655-03-5
Product Number: AG006O7D(AGN-PC-07CLYZ)
Synonyms:
MDL No: MFCD09260454
Molecular Formula: C16H13BO2
Molecular Weight: 248.0842

Identification/Properties

Properties
BP:
463 °C at 760 mmHg.
Storage:
2-8℃;Inert atmosphere;
Form:
Solid
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:
287
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


4-(2-Naphthyl)benzeneboronic acid, also known as Naphthylboronic Acid, is a versatile compound widely used in chemical synthesis. With its unique structure and reactivity, this compound serves as a key building block in the preparation of a variety of organic molecules. In particular, 4-(2-Naphthyl)benzeneboronic acid is commonly utilized in Suzuki-Miyaura cross-coupling reactions, a powerful method for forming carbon-carbon bonds in organic compounds. This reaction, catalyzed by palladium, enables the efficient synthesis of biaryl compounds, which are prevalent in pharmaceuticals, agrochemicals, and materials science. Additionally, Naphthylboronic Acid can be employed in the functionalization of aromatic systems, allowing chemists to introduce specific functional groups at precise positions in the molecule. Its compatibility with various reaction conditions and its ability to undergo selective transformations make 4-(2-Naphthyl)benzeneboronic acid a valuable tool for synthetic chemists seeking to design and produce complex organic molecules with specific properties.