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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, [3-(2,5-dihydro-2,5-dioxo-1H-pyrrol-1-yl)phenyl]-

O=C1C=CC(=O)N1c1cccc(c1)B(O)O Request for Quotation
Chemical Name: Boronic acid, [3-(2,5-dihydro-2,5-dioxo-1H-pyrrol-1-yl)phenyl]-
CAS Number: 170368-42-0
Product Number: AG00HZE3(AGN-PC-03S3NZ)
Synonyms:
MDL No:
Molecular Formula: C10H8BNO4
Molecular Weight: 216.98582

Identification/Properties

Computed Properties
Molecular Weight:
216.987g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
2
Exact Mass:
217.055g/mol
Monoisotopic Mass:
217.055g/mol
Topological Polar Surface Area:
77.8A^2
Heavy Atom Count:
16
Formal Charge:
0
Complexity:
324
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

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Chemical Structure


The molecule (3-(2,5-Dioxo-2,5-dihydro-1H-pyrrol-1-yl)phenyl)boronic acid, also known as $name$, is a versatile compound widely used in chemical synthesis. One of its key applications is as a reagent in Suzuki-Miyaura cross-coupling reactions. This reaction is vital in the formation of carbon-carbon bonds, allowing for the synthesis of complex organic molecules. $name$ acts as a boronic acid source, participating in the coupling reaction with various halide or pseudohalide substrates under palladium catalysis. This process enables the construction of diverse molecular scaffolds with high efficiency and selectivity, making $name$ an essential tool in modern organic synthesis.