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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, [4-(1-pyrenyl)phenyl]-

OB(c1ccc(cc1)c1ccc2c3c1ccc1c3c(cc2)ccc1)O Request for Quotation
Chemical Name: Boronic acid, [4-(1-pyrenyl)phenyl]-
CAS Number: 872050-52-7
Product Number: AG004N2G(AGN-PC-0CS061)
Synonyms:
MDL No:
Molecular Formula: C22H15BO2
Molecular Weight: 322.1643

Identification/Properties

Properties
Storage:
2-8℃;Inert atmosphere;
Form:
Solid
Computed Properties
Molecular Weight:
322.17g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
2
Exact Mass:
322.117g/mol
Monoisotopic Mass:
322.117g/mol
Topological Polar Surface Area:
40.5A^2
Heavy Atom Count:
25
Formal Charge:
0
Complexity:
473
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:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


(4-(Pyren-1-yl)phenyl)boronic acid is a versatile chemical compound widely used in organic synthesis. It serves as a crucial building block in the construction of various functional materials and complex molecules due to its unique properties and reactivity. In chemical synthesis, this compound acts as a valuable reagent for Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in a controlled and efficient manner. This reaction is pivotal in the formation of biaryl compounds, which find applications in pharmaceuticals, materials science, and organic electronics. Additionally, (4-(Pyren-1-yl)phenyl)boronic acid can be utilized in the preparation of luminescent materials, sensor molecules, and conjugated polymers, highlighting its significance in the development of advanced functional materials. Its ability to undergo various chemical transformations makes it a valuable tool for researchers and chemists seeking to access and modify complex molecules for a wide range of applications.