CAS 794-94-5
:Benzoic acid, 4-methoxy-, 1,1′-anhydride
- (4-Methoxybenzoyl) 4-methoxybenzoate
- 4-Methoxybenzoic acid anhydride
- Benzoic acid, 4-methoxy-, 1,1′-anhydride
- Benzoic acid, 4-methoxy-, anhydride
- NSC 101011
- p-Anisic acid anhydride
- p-Anisic anhydride
- p-Methoxybenzoic anhydride
4-Methoxybenzoic anhydride, 98%
CAS:4-Methoxybenzoic anhydride is used as pharmaceutical intermediates. This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU refer
Formula:C16H14O5Purity:98%Color and Shape:White, Crystals or powder or crystalline powderMolecular weight:286.284-Methoxybenzoic anhydride
CAS:Formula:C16H14O5Purity:97%Color and Shape:SolidMolecular weight:286.27944-Methoxybenzoic Anhydride
CAS:Formula:C16H14O5Purity:>97.0%(GC)(T)Color and Shape:White to Light yellow powder to crystalMolecular weight:286.284-Methoxybenzoic anhydride
CAS:4-Methoxybenzoic anhydride is a nonsteroidal anti-inflammatory drug (NSAID) that has a hydroxy group, which makes it susceptible to nucleophilic attack. The reaction mechanism of 4-methoxybenzoic anhydride involves hydroxyl group and phosphorus pentachloride. Kinetic data for the reaction was obtained from kinetic studies. The kinetic study found that the rate of the reaction increased with increasing concentration of amines and amides in the reaction mixture. 4-Methoxybenzoic anhydride has been shown to have antiinflammatory activity in various tests on animals, including rats, guinea pigs, and rabbits. The mechanism of this activity may be due to its ability to inhibit prostaglandin synthesis by blocking cyclooxygenase enzyme activity.
Formula:C16H14O5Purity:Min. 95%Color and Shape:PowderMolecular weight:286.28 g/molp-Anisic anhydride
CAS:Formula:C16H14O5Purity:97%+(GC-MS);RGColor and Shape:Crystalline PowderMolecular weight:286.283






