Iminas

Applications Dibromoformaldoxime is a reagent that undergoes cycloaddition with alkynes to prepare substituted 3-bromo-isoxazoles in high yield.
References Chiarino, D., et al.: J. Heterocyclic Chem., 24, 43 (1987); De Amici, M., et al.: J. Org. Chem., 54, 2646 (1989); Castelhano, A., et al.: 16, 335 (1988).

Applications Dimethylglyoxime is a chelating agent which forms complexes with metals such as copper, nickel, and palladium..
Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package

Applications Benzamide Oxime is used to prepare aryloxadiazoles as apoptosis inducers and anticancer agents. It is also used in the synthesis of aryloxadiazolyltropane analogs of cocaine.
Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package
References Zhang, H., et al.: J. Med. Chem., 48, 5215 (2005); Carroll, F., et al.: J. Med. Chem., 36, 2886 (1993)

Applications Reagent used to prepare poly-substituted benzenes.
References Grady, R., et al.: J. Cell. Biochem., 25, 15 (1984), Powis, G., et al.: Cancer Res., 47, 2363 (1987), Zeiger, E., et al.: Environ. Mol. Mut., 11, 1 (1988),

Applications Acetone oxime was one of the reagents used as a part of preparation of arylbenzoxazoles as potent and selective estrogen receptor-β ligands.
Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package
References Malamas, M., et al.: J. Med. Chem., 47, 5021 (2004)

Syringaldoxime is a tyrosinase inhibitor that inhibits the production of melanin. It is used in the treatment of vitiligo, a skin condition characterized by patches of depigmented skin. Syringaldoxime binds to benzal-dioxime and inhibits its activity. This inhibition leads to decreased production of hydroxytyrosine, which is an important intermediate in the synthesis of melanin. It also has inhibitory activity against l-dopa oxidation and enzyme catalyzed reactions. Syringaldoxime has two moieties, tropolone and methoxy, which are responsible for its inhibitory effects on tyrosinase activity.

3,4-Dichlorobenzaldehyde oxime is a natural carotenoid that has been shown to have antibacterial activity. 3,4-Dichlorobenzaldehyde oxime is produced by the reaction of malonate and aldehyde in an incubated system. This compound has been shown to be active against Gram-positive bacteria such as staphylococcus and aldoximes and Gram-negative bacteria such as E. coli, Salmonella typhimurium, and Shigella flexneri. 3,4-Dichlorobenzaldehyde oxime inhibits bacterial growth by binding to the 50S ribosomal subunit of the bacterial cell membrane. This binding prevents protein synthesis, leading to cell death. The biosynthesis of 3,4-dichlorobenzaldehyde oxime involves the conversion of abscisic acid (ABA) into ABA quinone through oxidation by an enzyme called ABA oxidase

4-(N,N-Dimethylamino)benzaldoxime is an efficient method for the detection of cinnamic acid and its esters. It reacts with aldehydes to form 4-nitrosobenzaldehyde products that are detectable by ultraviolet spectroscopy. The reaction takes place in aqueous solutions with a pH range of 5-8 and is catalyzed by an enzyme called carboxylate. This reaction has been shown to be useful for the detection of cinnamic acid and its esters in food, tobacco smoke, and other samples.

4-Bromo-2-fluorobenzaldoxime is a fine chemical that is used as a building block in the synthesis of complex molecules. It is also an intermediate in the production of pharmaceuticals, research chemicals, and other specialty chemicals. 4-Bromo-2-fluorobenzaldoxime has a CAS number of 202865-64-3 and is a useful reagent for organic synthesis. It can be used to produce high quality compounds with versatile building blocks.