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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)-

Benzene, 1-bromo-2-fluoro-3-(trifluoromethyl)-

Brc1cccc(c1F)C(F)(F)F Request for Quotation
Chemical Name: Benzene, 1-bromo-2-fluoro-3-(trifluoromethyl)-
CAS Number: 144584-67-8
Product Number: AG001JSR(AGN-PC-0KK7QM)
Synonyms:
MDL No:
Molecular Formula: C7H3BrF4
Molecular Weight: 242.9963

Identification/Properties

Computed Properties
Molecular Weight:
242.999g/mol
XLogP3:
3.6
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
0
Exact Mass:
241.935g/mol
Monoisotopic Mass:
241.935g/mol
Topological Polar Surface Area:
0A^2
Heavy Atom Count:
12
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:
H227-H315-H319-H335
Precautionary Statements:
P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


3-Bromo-2-fluorobenzotrifluoride is a versatile chemical reagent commonly employed in organic synthesis. Its unique chemical structure facilitates its use in various reactions, making it a valuable tool for chemists. This compound is particularly prized for its ability to selectively substitute the bromine and fluorine atoms in aromatic compounds, leading to the synthesis of complex molecules with precise substitutions. In organic chemistry, it is frequently used as a building block in the creation of pharmaceuticals, agrochemicals, and advanced materials. Additionally, 3-Bromo-2-fluorobenzotrifluoride plays a crucial role in the development of new synthetic methodologies, providing chemists with opportunities to explore innovative routes to synthesizing novel compounds. Its application in chemical synthesis extends to the realms of medicinal chemistry, material science, and chemical research, highlighting its significance in the advancement of diverse fields.