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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-5-chloro-2-fluoro-4-methyl-

Clc1cc(Br)c(cc1C)F Request for Quotation
Chemical Name: Benzene, 1-bromo-5-chloro-2-fluoro-4-methyl-
CAS Number: 93765-83-4
Product Number: AG006EBJ(AGN-PC-0KK7O4)
Synonyms:
MDL No: MFCD00236592
Molecular Formula: C7H5BrClF
Molecular Weight: 223.4700

Identification/Properties

Properties
BP:
221.1 °C at 760 mmHg
Storage:
Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
223.469g/mol
XLogP3:
3.7
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
0
Exact Mass:
221.925g/mol
Monoisotopic Mass:
221.925g/mol
Topological Polar Surface Area:
0A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
120
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


1-Bromo-5-chloro-2-fluoro-4-methylbenzene is a highly versatile compound that serves as a valuable building block in chemical synthesis. This compound is commonly used in organic chemistry reactions, particularly in the field of drug discovery and development.Its unique combination of bromine, chlorine, fluorine, and methyl groups provides various opportunities for structural modification and functional group transformations. The presence of the halogen atoms (bromine, chlorine, and fluorine) allows for selective reactions, such as substitution and cross-coupling reactions, leading to the synthesis of complex molecules with specific biological activities.The methyl group adds steric effects and influences the compound's reactivity and stability. Furthermore, the substituted benzene ring provides a conjugated system that can participate in aromatic substitution reactions, aromatic electrophilic additions, and other important synthetic pathways.In conclusion, 1-Bromo-5-chloro-2-fluoro-4-methylbenzene plays a crucial role in the synthesis of pharmaceuticals, agrochemicals, and materials with tailored properties, making it a valuable tool for chemists engaged in synthetic organic chemistry research.