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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)-

(3-methoxycarbonyl-5-nitrophenyl)boronic acid

COC(=O)c1cc(cc(c1)[N+](=O)[O-])B(O)O Request for Quotation
Chemical Name: (3-methoxycarbonyl-5-nitrophenyl)boronic acid
CAS Number: 117342-20-8
Product Number: AG000E5Q(AGN-PC-0KKVH2)
Synonyms:
MDL No:
Molecular Formula: C8H8BNO6
Molecular Weight: 224.9632

Identification/Properties

Computed Properties
Molecular Weight:
224.963g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
6
Rotatable Bond Count:
3
Exact Mass:
225.044g/mol
Monoisotopic Mass:
225.044g/mol
Topological Polar Surface Area:
113A^2
Heavy Atom Count:
16
Formal Charge:
0
Complexity:
278
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


$Name$ presents a versatile tool for chemical synthesis due to its distinctive properties. One of its key applications is in Suzuki-Miyaura cross-coupling reactions, where it acts as a pivotal building block in forming carbon-carbon bonds. The (3-(Methoxycarbonyl)-5-nitrophenyl)boronic acid serves as a valuable reagent in the preparation of various organic compounds, making it indispensable in the field of medicinal chemistry and material science. Its exceptional stability, reactivity, and compatibility with a wide range of functional groups make it a preferred choice for synthetic chemists seeking to efficiently craft complex molecular structures.