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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-fluoro-2-(trifluoromethyl)phenyl]boronic acid

Fc1ccc(c(c1)B(O)O)C(F)(F)F Request for Quotation
Chemical Name: [5-fluoro-2-(trifluoromethyl)phenyl]boronic acid
CAS Number: 928053-97-8
Product Number: AG00GS6J(AGN-PC-04TKR9)
Synonyms:
MDL No:
Molecular Formula: C7H5BF4O2
Molecular Weight: 207.9180

Identification/Properties

Properties
MP:
146-150ºC
BP:
271.4°C at 760 mmHg
Storage:
Inert atmosphere;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
207.919g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
6
Rotatable Bond Count:
1
Exact Mass:
208.032g/mol
Monoisotopic Mass:
208.032g/mol
Topological Polar Surface Area:
40.5A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
197
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#:
-
Hazard Statements:
H302
Precautionary Statements:
P280-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


$Name$ is a versatile chemical compound commonly used in chemical synthesis as a critical building block. Its unique properties make it a valuable tool in the creation of various pharmaceuticals, agrochemicals, and materials. In particular, 5-Fluoro-2-(trifluoromethyl)phenylboronic acid is prized for its ability to facilitate Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds under mild conditions. This compound serves as a key reagent in the preparation of complex organic molecules, making it indispensable in the field of organic chemistry. Additionally, its trifluoromethyl group enhances the overall reactivity and selectivity of the reactions it undergoes, further solidifying its importance in modern chemical synthesis practices.