CAS 182056-39-9
:2-Bromo-4-iodo-1-methoxybenzene
Description:
2-Bromo-4-iodo-1-methoxybenzene, with the CAS number 182056-39-9, is an organic compound that belongs to the class of halogenated aromatic compounds. It features a benzene ring substituted with a methoxy group (-OCH3), a bromine atom (Br), and an iodine atom (I) at specific positions, making it a polyhalogenated derivative. The presence of both bromine and iodine introduces significant reactivity, particularly in nucleophilic substitution reactions. The methoxy group enhances the electron density of the aromatic ring, influencing its reactivity and stability. This compound is typically used in organic synthesis and may serve as an intermediate in the production of pharmaceuticals, agrochemicals, or other complex organic molecules. Its physical properties, such as melting point, boiling point, and solubility, can vary based on the specific conditions and purity of the sample. Safety precautions should be taken when handling this compound, as both bromine and iodine are hazardous substances.
Formula:C7H6BrIO
InChI:InChI=1S/C7H6BrIO/c1-10-7-3-2-5(9)4-6(7)8/h2-4H,1H3
SMILES:COc1ccc(cc1Br)I
Synonyms:- 2-Bromo-4-iodoanisole
- 2-Bromo-4-iodophenyl methyl ether
- 2-Bromo-4-iodo anisole
- 2-Bromo-4-Iodo-1-Methoxy-Benzene
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Found 4 products.
Benzene, 2-bromo-4-iodo-1-methoxy-
CAS:Formula:C7H6BrIOPurity:95%Color and Shape:SolidMolecular weight:312.93042-Bromo-4-iodoanisole
CAS:2-Bromo-4-iodoanisoleFormula:C7H6BrIOPurity:≥95%Color and Shape: off-white to faint gray crystalline crystalline powderMolecular weight:312.93g/mol2-Bromo-4-iodoanisole
CAS:<p>2-Bromo-4-iodoanisole is an electrophilic intermediate that can be synthetically prepared by regioselective halogenations of 4-iodoanisole. It is also a substrate for sequential halogenations with bromine or iodine. The 2-bromo-4-iodoanisole reacts with aluminum to form an aluminate, which can be used as a catalyst in organic synthesis. 2-Bromo-4-iodoanisole has been shown to react with aromatic rings by electrophilically attacking the ring and adding a second bromine atom to the ring, leading to quenching of the molecule and formation of structurally diverse products.</p>Formula:C7H6BrIOPurity:Min. 95%Molecular weight:312.93 g/mol



