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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)-

(2-methoxy-4-nitrophenyl)boronic acid

COc1cc(ccc1B(O)O)[N+](=O)[O-] Request for Quotation
Chemical Name: (2-methoxy-4-nitrophenyl)boronic acid
CAS Number: 949892-13-1
Product Number: AG00IIO6(AGN-PC-0BZ184)
Synonyms:
MDL No:
Molecular Formula: C7H8BNO5
Molecular Weight: 196.95312

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


(2-Methoxy-4-nitrophenyl)boronic acid is a versatile and valuable boronic acid derivative that finds widespread applications in chemical synthesis, particularly in the field of organic chemistry. This compound serves as a key building block in the formation of various functional molecules and pharmaceutical intermediates due to its unique reactivity and compatibility with a variety of organic reactions.In chemical synthesis, (2-Methoxy-4-nitrophenyl)boronic acid is commonly used as a cross-coupling reagent in Suzuki-Miyaura coupling reactions. This powerful palladium-catalyzed coupling reaction allows for the formation of carbon-carbon bonds between an aryl or vinyl halide and an organoboronic acid, such as (2-Methoxy-4-nitrophenyl)boronic acid. This process enables chemists to efficiently construct complex organic molecules with precision and control.Moreover, (2-Methoxy-4-nitrophenyl)boronic acid can participate in other types of transformations, such as borylation reactions, which involve the conversion of the boronic acid group into other functional groups like aryl halides or phenols. This versatility makes (2-Methoxy-4-nitrophenyl)boronic acid a valuable tool for the synthesis of a wide range of chemical compounds, including pharmaceuticals, agrochemicals, and materials.Overall, the application of (2-Methoxy-4-nitrophenyl)boronic acid in chemical synthesis offers chemists a reliable and effective method for the construction of diverse organic molecules with important implications for drug discovery, materials science, and other industrial applications.