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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-5-(trifluoromethyl)phenyl]-

OB(c1cc(ccc1Cl)C(F)(F)F)O Request for Quotation
Chemical Name: Boronic acid, [2-chloro-5-(trifluoromethyl)phenyl]-
CAS Number: 182344-18-9
Product Number: AG0023P1(AGN-PC-0KL1TB)
Synonyms:
MDL No: MFCD00797335
Molecular Formula: C7H5BClF3O2
Molecular Weight: 224.3726

Identification/Properties

Properties
MP:
108℃
BP:
303.2±52.0°C at 760 mmHg
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-5-(trifluoromethyl)phenylboronic Acid, containing varying amounts of Anhydride, is a versatile compound widely used in chemical synthesis. This compound serves as a key building block in organic chemistry reactions, particularly in the field of pharmaceuticals and agrochemicals. Its unique structure and reactivity make it an essential reagent for creating complex molecules with specific properties. In synthesis, this compound is commonly employed as a key intermediate in the preparation of various biologically active compounds and materials. Its utility extends to the formation of carbon-carbon, carbon-nitrogen, and carbon-oxygen bonds, enabling the efficient construction of diverse molecular structures. Furthermore, the presence of the trifluoromethyl group enhances the compound's stability and lipophilicity, making it an ideal candidate for use in drug discovery and material science applications.