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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, 2-anthracenyl-

OB(c1ccc2c(c1)cc1c(c2)cccc1)O Request for Quotation
Chemical Name: Boronic acid, 2-anthracenyl-
CAS Number: 141981-64-8
Product Number: AG001HI0(AGN-PC-0MUN1O)
Synonyms:
MDL No: MFCD07784001
Molecular Formula: C14H11BO2
Molecular Weight: 222.0469

Identification/Properties

Properties
BP:
479.5°C at 760 mmHg
Storage:
Inert atmosphere;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
222.05g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
1
Exact Mass:
222.085g/mol
Monoisotopic Mass:
222.085g/mol
Topological Polar Surface Area:
40.5A^2
Heavy Atom Count:
17
Formal Charge:
0
Complexity:
269
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:
H302-H315-H319-H332-H335
Precautionary Statements:
P261-P280-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


Anthracen-2-ylboronic acid is a versatile compound widely utilized in chemical synthesis as a key building block for creating novel organic molecules. In organic chemistry, it serves as a vital reagent for the formation of carbon-carbon and carbon-heteroatom bonds through various cross-coupling reactions. This compound finds application in the preparation of pharmaceuticals, agrochemicals, and materials science, where the selective functionalization of aromatic systems is crucial. Additionally, Anthracen-2-ylboronic acid is employed in the development of advanced materials such as organic light-emitting diodes (OLEDs) and organic semiconductors, highlighting its significance in modern synthetic chemistry practices.