Imines

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 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 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 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)

Benzamidoxime hydrochloride is an activator that can be used in the synthesis of 6-membered alkylaryl compounds. It contains a six-membered amidine ring and a six-membered ring.

a-Benzoin oxime is a molecule that has been synthesized and characterized by nuclear magnetic resonance (NMR) spectroscopy. The compound contains a hydroxy group, which is responsible for the vibrational mode observed in anhydrous acetonitrile, sodium citrate and galleria mellonella. This molecule also has a metal ion which coordinates with the hydroxyl group of the benzoin oxime. The coordination complex is formed in an enzyme preparation containing p. aeruginosa and molybdenum as the metal ion.

2-Naphthaldehyde oxime is a reactive aldoxime that can be used as an oxidant in organic chemistry. It is able to increase the rate of hydrolysis by acid catalysts, and has been shown to cause biomolecular damage due to its ability to react with functional groups such as amines and alcohols. 2-Naphthaldehyde oxime reacts with silicon, styrene, and polystyrene. The reaction produces carbon dioxide, hydrogen, and water. This product also has the capability of solvating organic compounds through the use of water molecules. Hypervalent oxidation reactions may occur with 2-naphthaldehyde oxime due to its ability to form multiple bonds with oxygen atoms.

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.

2-Oxopropanal oxime is a coordination compound that has been shown to be an effective catalyst for the oxidation of hydrochloric acid to hydrogen chloride and methane. It has also been found to have a protective effect against the nerve agent sarin. 2-Oxopropanal oxime binds to the active site of the enzyme acetylcholinesterase, which breaks down acetylcholine, preventing its action on muscle cells and leading to paralysis. The reaction mechanism of 2-Oxopropanal oxime is not well understood, but it is hypothesized that it may involve a pyridinium intermediate. This compound has been investigated as a possible treatment for metabolic disorders, such as obesity and type II diabetes, due to its ability to stimulate detoxification enzymes in the liver. 2-Oxopropanal oxime is also used in plant biotechnology as an expression plasmid because it allows plants to produce large quantities of proteins with signal pept

(S)-(+)-Methyl phenyl sulfoximine, or MMPS, is a synthetic chiral organocatalyst that has been shown to be a highly effective catalyst for the asymmetric synthesis of benzothiazines. It is used in a variety of reactions including cross-coupling, catalytic asymmetric synthesis, desymmetrization and solvents. MMPS has been shown to be enantiopure and stereochemically pure. The yield of this reaction using MMPS as a catalyst was about 98%.