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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)-

Boronicacid, B-(2-methyl-3,5-dinitrophenyl)-

[O-][N+](=O)c1cc(B(O)O)c(c(c1)[N+](=O)[O-])C Request for Quotation
Chemical Name: Boronicacid, B-(2-methyl-3,5-dinitrophenyl)-
CAS Number: 24341-76-2
Product Number: AG007NS1(AGN-PC-0L9OY0)
Synonyms:
MDL No:
Molecular Formula: C7H7BN2O6
Molecular Weight: 225.9513

Identification/Properties

Computed Properties
Molecular Weight:
225.951g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
6
Rotatable Bond Count:
1
Exact Mass:
226.04g/mol
Monoisotopic Mass:
226.04g/mol
Topological Polar Surface Area:
132A^2
Heavy Atom Count:
16
Formal Charge:
0
Complexity:
288
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-H335
Precautionary Statements:
P261-P280-P301+P312-P302+P352-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


The (3,5-Dinitro-2-methylphenyl)boronic acid is a versatile compound widely used in organic synthesis due to its unique reactivity and ability to serve as a valuable building block in the creation of various organic molecules. In chemical synthesis, this compound acts as a key component in Suzuki-Miyaura cross-coupling reactions, where it functions as a boronate ester to facilitate the formation of carbon-carbon bonds. Its selective reactivity makes it an essential tool in the construction of complex organic structures, enabling chemists to access a wide range of functionalized compounds. Additionally, the (3,5-Dinitro-2-methylphenyl)boronic acid can be employed in the development of pharmaceuticals, agrochemicals, and materials science, highlighting its significance in the field of modern organic chemistry.