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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-Methyl-3-(trifluoromethyl)phenylboronic acid

OB(c1cccc(c1C)C(F)(F)F)O Request for Quotation
Chemical Name: 2-Methyl-3-(trifluoromethyl)phenylboronic acid
CAS Number: 947533-86-0
Product Number: AG0068HD(AGN-PC-078TDJ)
Synonyms:
MDL No:
Molecular Formula: C8H8BF3O2
Molecular Weight: 203.9541

Identification/Properties

Properties
BP:
282.6°C at 760 mmHg
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
203.955g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
1
Exact Mass:
204.057g/mol
Monoisotopic Mass:
204.057g/mol
Topological Polar Surface Area:
40.5A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
196
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


2-Methyl-3-trifluoromethylphenylboronic acid, also known as $name$, is a versatile chemical reagent commonly used in organic synthesis. This compound plays a crucial role as a boronic acid derivative in various chemical reactions. One of the key applications of $name$ is its use as a boronic acid building block in Suzuki-Miyaura cross-coupling reactions. In this process, $name$ can react with aryl halides or pseudohalides in the presence of a palladium catalyst to form biaryl compounds. This powerful reaction has found widespread use in the pharmaceutical industry for the synthesis of complex organic molecules, including drug candidates and natural products. Additionally, $name$ can also participate in other types of organic transformations, such as C-H activation, halogenation, and functional group interconversion, making it a valuable tool for synthetic chemists in the development of new chemical entities and materials.