![1,1′-Oxybis[4-iodobenzene]](/_next/image/?url=https%3A%2Fstatic.cymitquimica.com%2Fcas-image%2Fthumb-webp%2F79152-11-oxybis-4-iodobenzene.webp&w=3840&q=75)
CAS 28896-49-3: 1,1′-Oxybis[4-iodobenzene]
Formula:C12H8I2O
InChI:InChI=1S/C12H8I2O/c13-9-1-5-11(6-2-9)15-12-7-3-10(14)4-8-12/h1-8H
InChI key:InChIKey=VHEGXFQQYZIMMF-UHFFFAOYSA-N
SMILES:O(C1=CC=C(I)C=C1)C2=CC=C(I)C=C2
Synonyms:- 1,1'-Oxybis(4-Iodobenzene)
- 1-Iodo-4-(4-iodophenoxy)benzene
- 1-Iodo-4-Phenoxybenzene
- 4,4′-Diiododiphenyl ether
- 4,4′-Diiodophenyl ether
- 4,4′-Oxybis(iodobenzene)
- 4-Iodophenyl ether
- Benzene, 1,1′-oxybis[4-iodo-
- Bis(4-iodophenyl)ether
- Bis(p-iodophenyl) ether
- Ether, bis(p-iodophenyl)
- See more synonyms
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Found 4 products.
Benzene, 1,1'-oxybis[4-iodo-
CAS:Formula:C12H8I2OPurity:95%Color and Shape:SolidMolecular weight:422.00034-Iodophenyl ether
CAS:4-Iodophenyl ether is a chemical compound that can be synthesized from the reaction of an aromatic hydrocarbon with ethoxycarbonyl iodide and palladium catalysts. The reaction is typically conducted in the presence of aluminium chloride as a catalyst at elevated temperature (200-250 degrees Celsius) for 3-4 hours. This process produces a mixture of 4-iodophenyl ether and 4-iodophenyl acetate, which can be separated by distillation. This product has been used in organic reactions such as the synthesis of various heterocycles, including pyrrole, furan, thiophene, and indole. It has also been used to introduce carbonyl groups into organic molecules.Formula:C12H8I2OPurity:Min. 95%Molecular weight:422 g/mol