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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, 5-bromo-2-(bromomethyl)-1,3-difluoro-

BrCc1c(F)cc(cc1F)Br Request for Quotation
Chemical Name: Benzene, 5-bromo-2-(bromomethyl)-1,3-difluoro-
CAS Number: 162744-60-7
Product Number: AG001TEH(AGN-PC-0KKVC7)
Synonyms:
MDL No:
Molecular Formula: C7H4Br2F2
Molecular Weight: 285.9115

Identification/Properties

Properties
BP:
243.5°C at 760 mmHg
Storage:
Inert atmosphere;2-8℃;
Form:
Liquid
Computed Properties
Molecular Weight:
285.914g/mol
XLogP3:
3.4
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
1
Exact Mass:
285.863g/mol
Monoisotopic Mass:
283.865g/mol
Topological Polar Surface Area:
0A^2
Heavy Atom Count:
11
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


4-Bromo-2,6-difluorobenzyl bromide is a versatile chemical compound widely used in chemical synthesis processes. With its unique molecular structure, this compound plays a crucial role in the creation of various pharmaceuticals, agrochemicals, and advanced materials.One of the key applications of 4-Bromo-2,6-difluorobenzyl bromide is as a valuable building block in the synthesis of complex organic molecules. Its bromide functional group serves as a reactive site for introducing new chemical moieties into target molecules, enabling chemists to modify and tailor the properties of these compounds for specific applications.In addition, 4-Bromo-2,6-difluorobenzyl bromide is often utilized as a key intermediate in the production of specialized reagents and catalysts. Its ability to undergo diverse chemical reactions under controlled conditions makes it an essential component in the development of new synthetic methodologies and efficient routes for preparing intricate molecular structures.Furthermore, the unique reactivity of 4-Bromo-2,6-difluorobenzyl bromide allows chemists to access a wide range of functionalized derivatives with enhanced properties such as increased stability, solubility, and bioactivity. By harnessing the synthetic potential of this compound, researchers can explore novel chemical transformations and design innovative molecules with improved performance characteristics.