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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-Ethoxy-6-fluorophenylboronic acid

CCOc1cccc(c1B(O)O)F Request for Quotation
Chemical Name: 2-Ethoxy-6-fluorophenylboronic acid
CAS Number: 957062-68-9
Product Number: AG00IJDM(AGN-PC-00UQGB)
Synonyms:
MDL No:
Molecular Formula: C8H10BFO3
Molecular Weight: 183.9726

Identification/Properties

Computed Properties
Molecular Weight:
183.973g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
3
Exact Mass:
184.071g/mol
Monoisotopic Mass:
184.071g/mol
Topological Polar Surface Area:
49.7A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
156
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:
P233-P260-P261-P264-P270-P271-P280-P301+P312-P302+P352-P304-P304+P340-P305+P351+P338-P312-P321-P330-P332+P313-P337+P313-P340-P362-P403-P403+P233-P405-P501
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


2-Ethoxy-6-fluorophenylboronic acid is a versatile compound commonly utilized in organic chemistry for its unique properties and reactivity. This compound serves as a crucial building block in the synthesis of various pharmaceuticals, agrochemicals, and materials due to its boronic acid functionality. In chemical synthesis, 2-Ethoxy-6-fluorophenylboronic acid acts as a key reagent in Suzuki-Miyaura cross-coupling reactions, a widely-used method for forming carbon-carbon bonds. This enables the introduction of the 2-ethoxy-6-fluorophenyl group into complex molecular structures, providing an efficient route for the construction of diverse organic compounds. Furthermore, the presence of the fluorine atom in 2-Ethoxy-6-fluorophenylboronic acid imparts unique properties to the resulting molecules, such as enhanced stability and altered electronic properties, making it a valuable tool for customizing the physical and chemical characteristics of the final products. Overall, the application of 2-Ethoxy-6-fluorophenylboronic acid in chemical synthesis offers chemists a powerful tool for the controlled and precise construction of complex organic molecules with tailored functionalities and properties.