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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)-

Boronic acid, [2-chloro-4-(trifluoromethyl)phenyl]-

OB(c1ccc(cc1Cl)C(F)(F)F)O Request for Quotation
Chemical Name: Boronic acid, [2-chloro-4-(trifluoromethyl)phenyl]-
CAS Number: 254993-59-4
Product Number: AG00337O(AGN-PC-0KL27Y)
Synonyms:
MDL No: MFCD02684337
Molecular Formula: C7H5BClF3O2
Molecular Weight: 224.3726

Identification/Properties

Properties
MP:
110-112°C
Storage:
Inert atmosphere;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
224.37g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
1
Exact Mass:
224.002g/mol
Monoisotopic Mass:
224.002g/mol
Topological Polar Surface Area:
40.5A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
200
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


2-Chloro-4-(Trifluoromethyl)Benzeneboronic Acid is a versatile chemical compound widely utilized in chemical synthesis processes. One of its key applications is as a valuable building block in organic chemistry, particularly in the field of Suzuki-Miyaura cross-coupling reactions. This compound serves as a crucial reagent for the formation of carbon-carbon bonds, enabling the efficient and selective construction of complex organic molecules. By participating in these coupling reactions, 2-Chloro-4-(Trifluoromethyl)Benzeneboronic Acid facilitates the synthesis of a diverse range of pharmaceuticals, agrochemicals, and materials with enhanced properties. Its unique structure and reactivity make it an indispensable tool for researchers and scientists seeking to design novel compounds with specific functionalities and applications in various industries.