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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-chloro-3-nitrophenyl)-

OB(c1ccc(c(c1)[N+](=O)[O-])Cl)O Request for Quotation
Chemical Name: Boronic acid, (4-chloro-3-nitrophenyl)-
CAS Number: 151169-67-4
Product Number: AG001N57(AGN-PC-0LKZO0)
Synonyms:
MDL No: MFCD02258950
Molecular Formula: C6H5BClNO4
Molecular Weight: 201.3722

Identification/Properties

Computed Properties
Molecular Weight:
201.369g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
1
Exact Mass:
201g/mol
Monoisotopic Mass:
201g/mol
Topological Polar Surface Area:
86.3A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
198
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:
H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


Boronic acid, B-(4-chloro-3-nitrophenyl)-, is a versatile compound that finds widespread application in chemical synthesis. This specific boronic acid derivative is valued for its ability to participate in various organic reactions, particularly in the formation of carbon-carbon bonds through Suzuki-Miyaura cross-coupling reactions. When used as a reagent in organic synthesis, it facilitates the construction of complex molecular structures by enabling the selective arylation of various substrates.Furthermore, the presence of the 4-chloro-3-nitrophenyl group in this boronic acid derivative imparts unique electronic and steric properties, which can influence the reactivity and selectivity of the compound in synthetic transformations. Its strategic incorporation into molecular frameworks offers chemists a powerful tool for designing and accessing structurally diverse molecules with tailored properties.Overall, B-(4-chloro-3-nitrophenyl)-boronic acid stands as a valuable reagent in the toolkit of synthetic chemists, offering opportunities for the efficient construction of complex organic molecules and the exploration of novel chemical space.