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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, 1,1'-(1,2-ethanediyl)bis[2,3,4,5,6-pentabromo-

Brc1c(CCc2c(Br)c(Br)c(c(c2Br)Br)Br)c(Br)c(c(c1Br)Br)Br Request for Quotation
Chemical Name: Benzene, 1,1'-(1,2-ethanediyl)bis[2,3,4,5,6-pentabromo-
CAS Number: 84852-53-9
Product Number: AG003DBZ(AGN-PC-0NDYYY)
Synonyms:
MDL No:
Molecular Formula: C14H4Br10
Molecular Weight: 971.2216

Identification/Properties

Properties
MP:
345 °C
BP:
676.235°C at 760 mmHg
Storage:
Keep in dry area;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
971.226g/mol
XLogP3:
11.1
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
0
Rotatable Bond Count:
3
Exact Mass:
971.204g/mol
Monoisotopic Mass:
961.215g/mol
Topological Polar Surface Area:
0A^2
Heavy Atom Count:
24
Formal Charge:
0
Complexity:
352
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


1,2-Bis(perbromophenyl)ethane, also known as BPE, is a versatile compound commonly employed in chemical synthesis as a powerful brominating reagent. It is utilized primarily in the synthesis of various organic compounds, particularly in the bromination of aromatic rings.In organic chemistry, BPE serves as an efficient source of bromine atoms due to its high reactivity and selectivity towards aromatic systems. By reacting with a wide range of aromatic compounds, 1,2-Bis(perbromophenyl)ethane enables the introduction of bromine functionalities at specific positions on the aromatic ring. This selective bromination process is crucial for the synthesis of a variety of important intermediates used in the pharmaceutical, agrochemical, and material science industries.Moreover, the unique structure of BPE allows for controlled bromination reactions, leading to the formation of mono- or di-brominated products depending on the reaction conditions. This level of control is essential in the design and synthesis of complex organic molecules with precise substitution patterns.Overall, the application of 1,2-Bis(perbromophenyl)ethane in chemical synthesis highlights its significance as a valuable reagent for the preparation of brominated organic compounds with tailored properties and functionalities.