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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, [6-(1H-pyrrol-1-yl)-3-pyridinyl]-

OB(c1ccc(nc1)n1cccc1)O Request for Quotation
Chemical Name: Boronic acid, [6-(1H-pyrrol-1-yl)-3-pyridinyl]-
CAS Number: 899436-83-0
Product Number: AG00IFWC(AGN-PC-0ALU31)
Synonyms:
MDL No:
Molecular Formula: C9H9BN2O2
Molecular Weight: 187.99096

Identification/Properties

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 (6-(1H-Pyrrol-1-yl)pyridin-3-yl)boronic acid is a versatile and valuable reagent in chemical synthesis. This boronic acid derivative serves as a key building block in the formation of various organic compounds through Suzuki-Miyaura cross-coupling reactions. By acting as a coupling partner with suitable electrophiles in the presence of a palladium catalyst, this compound facilitates the creation of new carbon-carbon bonds. This methodology is commonly employed in the synthesis of pharmaceuticals, agrochemicals, and materials science, enabling the production of complex molecules with high efficiency and precision. The unique structural features of (6-(1H-Pyrrol-1-yl)pyridin-3-yl)boronic acid make it a valuable tool for organic chemists seeking to design and synthesize novel compounds for a range of applications.