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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-iodo-1,3-dimethyl-

Brc1cc(C)c(c(c1)C)I Request for Quotation
Chemical Name: Benzene, 5-bromo-2-iodo-1,3-dimethyl-
CAS Number: 206559-43-5
Product Number: AG002IKC(AGN-PC-0KK770)
Synonyms:
MDL No:
Molecular Formula: C8H8BrI
Molecular Weight: 310.9576

Identification/Properties

Properties
MP:
42 °C
BP:
282.4°C at 760 mmHg
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
310.96g/mol
XLogP3:
4
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
0
Rotatable Bond Count:
0
Exact Mass:
309.885g/mol
Monoisotopic Mass:
309.885g/mol
Topological Polar Surface Area:
0A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
104
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:
H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


5-Bromo-2-iodo-m-xylene is a versatile compound commonly used in chemical synthesis. This compound plays a crucial role in organic chemistry as a valuable building block for the creation of various complex molecules and pharmaceuticals. Its unique structure allows for strategic modifications that enable chemists to control and manipulate properties such as reactivity, bioavailability, and stability.In chemical synthesis, 5-Bromo-2-iodo-m-xylene can serve as a key intermediate in the preparation of a wide range of functionalized molecules. Its halogen atoms (bromine and iodine) provide sites for further derivatization, allowing for the introduction of different functional groups via various coupling reactions such as Suzuki coupling, Heck reaction, or nucleophilic substitution. This versatility makes it a valuable asset for designing and synthesizing new organic compounds with specific desired properties for applications in drug discovery, material science, and more.Additionally, the presence of both bromine and iodine atoms in the molecule enables chemists to fine-tune the electronic and steric properties of the resulting compounds. This precise control over the chemical structure can lead to improvements in the efficiency, selectivity, and overall success of the synthesis process. The use of 5-Bromo-2-iodo-m-xylene in chemical synthesis highlights its importance as a foundational reagent for achieving synthetic goals and advancing scientific research in the field of organic chemistry.