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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)-

5-Chloro-2-fluoro-4-methoxyphenylboronic acid

COc1cc(F)c(cc1Cl)B(O)O Request for Quotation
Chemical Name: 5-Chloro-2-fluoro-4-methoxyphenylboronic acid
CAS Number: 1072952-18-1
Product Number: AG007ERV(AGN-PC-0WABAA)
Synonyms:
MDL No:
Molecular Formula: C7H7BClFO3
Molecular Weight: 204.3911

Identification/Properties

Computed Properties
Molecular Weight:
204.388g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
2
Exact Mass:
204.016g/mol
Monoisotopic Mass:
204.016g/mol
Topological Polar Surface Area:
49.7A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
172
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:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


The (5-Chloro-2-fluoro-4-methoxyphenyl)boronic acid is a versatile chemical compound commonly used in organic synthesis as a key building block. This boronic acid derivative is highly valued for its ability to participate in various cross-coupling reactions, particularly in the field of palladium-catalyzed coupling reactions.In chemical synthesis, this compound acts as a valuable precursor in the formation of biaryl compounds through Suzuki-Miyaura coupling reactions. By serving as a nucleophilic partner in these reactions, it facilitates the formation of carbon-carbon bonds, enabling the construction of complex molecular structures with high efficiency.Furthermore, the (5-Chloro-2-fluoro-4-methoxyphenyl)boronic acid is often employed in medicinal chemistry for the synthesis of pharmaceutical intermediates and drug molecules. Its unique structural characteristics make it a valuable tool for introducing functional groups into molecules, thereby allowing for the fine-tuning of their biological activity and properties.Overall, the (5-Chloro-2-fluoro-4-methoxyphenyl)boronic acid plays a crucial role in modern organic synthesis as a versatile reagent with wide-ranging applications in the development of diverse chemical compounds, making it an indispensable tool for chemists engaged in the creation of novel molecules and materials.