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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)-

9H-fluoren-2-ylboronic acid

OB(c1ccc2c(c1)Cc1c2cccc1)O Request for Quotation
Chemical Name: 9H-fluoren-2-ylboronic acid
CAS Number: 480424-61-1
Product Number: AG003BZ7(AGN-PC-03IQBC)
Synonyms:
MDL No:
Molecular Formula: C13H11BO2
Molecular Weight: 210.0362

Identification/Properties

Properties
Storage:
Keep in dry area;2-8℃;

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


The organic compound (9H-Fluoren-2-yl)boronic acid, commonly referred to as Fluorenylboronic Acid, plays a pivotal role in chemical synthesis as a versatile building block. This unique compound is widely utilized in Suzuki-Miyaura cross-coupling reactions, which involve the coupling of boronic acids with organic halides or pseudohalides to form carbon-carbon bonds. This reaction is a fundamental tool in organic synthesis for the construction of complex molecules with high efficiency and selectivity. Fluorenylboronic acid's reactivity and stability make it a valuable reagent for the synthesis of pharmaceuticals, agrochemicals, and materials science applications. Its compatibility with a variety of functional groups and its ability to facilitate the formation of biaryl compounds make it a valuable asset in the toolbox of organic chemists.