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Halogenation, sulfonation, nitration or nitrosation of ethers, ether alcohols, ether phenols

Halogenation, sulfonation, nitration, or nitrosation of ethers, ether alcohols, and ether phenols involve the introduction of halogens, sulfonic acid groups, nitrates, or nitrosamines to the ether-based structures. Halogenation enhances the reactivity and stability of these compounds. Sulfonation adds water solubility and acidity. Nitration and nitrosation introduce nitro and nitrosamine functional groups, respectively. These modified ethers and ether derivatives offer tailored properties, opening new avenues for applications in research, materials science, and the development of specialized chemicals.

Products of Halogenation, sulfonation, nitration or nitrosation of ethers, ether alcohols, ether phenols
CAS No.Product NameMolecular Formula
101-80-44,4'-OxydianilineC12H12N2O
104-94-9p-AnisidineC7H9NO
107-30-2Chloromethyl methyl etherC2H5ClO
1163-19-5Decabromodiphenyl oxideC12Br10O
127-90-2Bis(2,3,3,3-tetrachloropropyl) etherC6H6Cl8O
13826-35-23-Phenoxybenzyl alcoholC13H12O2
174913-12-33-Bromo-5-chloroanisoleC7H6BrClO
2398-37-03-BromoanisoleC7H7BrO
32534-81-9Pentabromodiphenyl etherC12H5Br5O
6375-47-93'-Amino-4'-methoxyacetanilideC9H12N2O2
90-04-0o-AnisidineC7H9NO
91-23-62-NitroanisoleC7H7NO3
94-70-2o-PhenetidineC8H11NO
97-52-92-Methoxy-4-nitroanilineC7H8N2O3
97-53-0EugenolC10H12O2



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