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Halogenation, sulfonation, nitration or nitration of carboxylic anhydrides

The chemical modification of carboxylic anhydrides through halogenation, sulfonation, nitration, or nitrosation results in a group of compounds with distinctive properties and applications. These modifications introduce halogens, sulfonic acid groups, nitrates, or nitrosamine groups. The resultant derivatives are employed in various fields, such as flame retardants, pharmaceutical intermediates, and specialty chemicals. Halogenation enhances their reactivity and stability, while sulfonation adds water solubility and acidity. Nitration and nitrosation expand their applications in organic synthesis and chemical research. These modified carboxylic anhydrides offer tailored properties and diverse applications, contributing to advancements in chemistry and industry.

Products of Halogenation, sulfonation, nitration or nitration of carboxylic anhydrides
CAS No.Product NameMolecular Formula
106-31-0Butyric anhydrideC8H14O3
108-24-7Acetic anhydrideC4H6O3
108-30-5Succinic anhydrideC4H4O3
108-31-6Maleic anhydride C4H2O3
117-08-8Tetrachlorophthalic anhydrideC8Cl4O3
2051-49-2Hexanoic anhydrideC12H22O3
2421-28-53,3',4,4'-Benzophenonetetracarboxylic dianhydrideC17H6O7
24937-72-2Maleic Anhydride PolymersC4H2O3
26590-20-5Methyltetrahydrophthalic anhydride C9H10O3
552-30-71,2,4-Benzenetricarboxylic anhydrideC9H4O5
623-68-7Crotonic anhydrideC8H10O3
632-79-1Tetrabromophthalic anhydrideC8Br4O3
81-84-51,8-Naphthalic anhydrideC12H6O3
82-73-53-Bromophthalic anhydrideC8H3BrO3
923978-27-22-[2,6-Dimethyl-4-[(1E)-3-[4-(methylthio)phenyl]-3-oxo-1-propen-1-yl]phenoxy]-2-methylpropanoic acidC22H24O4S



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