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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)-

[4-propoxy-3-(trifluoromethyl)phenyl]boronic acid

CCCOc1ccc(cc1C(F)(F)F)B(O)O Request for Quotation
Chemical Name: [4-propoxy-3-(trifluoromethyl)phenyl]boronic acid
CAS Number: 1162257-45-5
Product Number: AG000BZ4(AGN-PC-0AC0ZD)
Synonyms:
MDL No:
Molecular Formula: C10H12BF3O3
Molecular Weight: 248.0067

Identification/Properties

Computed Properties
Molecular Weight:
248.008g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
6
Rotatable Bond Count:
4
Exact Mass:
248.083g/mol
Monoisotopic Mass:
248.083g/mol
Topological Polar Surface Area:
49.7A^2
Heavy Atom Count:
17
Formal Charge:
0
Complexity:
235
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 (4-Propoxy-3-(trifluoromethyl)phenyl)boronic acid is a versatile chemical reagent commonly used in organic synthesis. It serves as a key building block in the development of various pharmaceuticals, agrochemicals, and materials due to its unique properties and reactivity.In chemical synthesis, this compound is frequently employed in Suzuki-Miyaura cross-coupling reactions, where it acts as a boronic acid derivative to facilitate the formation of carbon-carbon bonds. By reacting with aryl halides or pseudohalides in the presence of a palladium catalyst, the (4-Propoxy-3-(trifluoromethyl)phenyl)boronic acid can be utilized to construct complex molecular structures with high efficiency and selectivity.Additionally, this boronic acid derivative can participate in other important transformations such as hydroxylation, arylation, and halogenation reactions, expanding its utility in the synthesis of diverse organic compounds. Its trifluoromethyl and propoxy functional groups further enhance its chemical compatibility and enable its incorporation into different molecular scaffolds with improved physicochemical properties.Overall, the (4-Propoxy-3-(trifluoromethyl)phenyl)boronic acid plays a crucial role in modern organic chemistry by enabling the construction of intricate and functionalized molecules, making it a valuable tool for synthetic chemists working in various research fields.