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Brc1cnc(nc1)C
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CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
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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, 4-bromo-2-(bromomethyl)-1-methoxy-

BrCc1cc(Br)ccc1OC Request for Quotation
Chemical Name: Benzene, 4-bromo-2-(bromomethyl)-1-methoxy-
CAS Number: 184970-28-3
Product Number: AG00AO3V(AGN-PC-0LK9CY)
Synonyms:
MDL No:
Molecular Formula: C8H8Br2O
Molecular Weight: 279.9565

Identification/Properties

Computed Properties
Molecular Weight:
279.959g/mol
XLogP3:
3.1
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
2
Exact Mass:
279.892g/mol
Monoisotopic Mass:
277.894g/mol
Topological Polar Surface Area:
9.2A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
119
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-(bromomethyl)-1-methoxybenzene, also known as $name$, is a versatile compound widely utilized in chemical synthesis for its unique reactivity and functional group compatibility. This compound serves as a valuable building block in the production of various organic compounds and materials due to its specific chemical properties.In chemical synthesis, 4-Bromo-2-(bromomethyl)-1-methoxybenzene is often employed as a key intermediate in the synthesis of pharmaceuticals, agrochemicals, and fine chemicals. Its bromine-containing functional groups provide opportunities for selective transformations, such as nucleophilic substitution reactions and cross-coupling reactions. The presence of a methoxy group enhances the compound's stability and facilitates certain synthetic pathways.Furthermore, the bromomethyl moiety in 4-Bromo-2-(bromomethyl)-1-methoxybenzene can serve as a masked reactive site, allowing for controlled release of the active bromine atom under specific reaction conditions. This feature enables precise modification of organic molecules and facilitates the synthesis of complex structures with desired functionalities.Overall, the application of 4-Bromo-2-(bromomethyl)-1-methoxybenzene in chemical synthesis offers a strategic approach to accessing diverse chemical space and designing novel compounds with tailored properties for various industrial and research purposes.