Iminas

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 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 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)

2,4-Dimethylbenzaldehyde oxime is a useful chemical for the synthesis of complex organic compounds. It is used as a research chemical and as a speciality chemical in the production of fine chemicals. 2,4-Dimethylbenzaldehyde oxime can be used as a versatile building block to form new compounds with different substituents. The compound has been shown to have high reactivity and good quality.

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.

3-Bromobenzaldoxime is a dialkylamino aldoxime compound that is soluble in organic solvents such as diethyl ether, chloroform, dichloromethane, and benzene. It can be synthesized from benzaldehyde and aniline through the reaction of cyclopentenes with phenylsulfonyl chloride. This reaction produces an intermediate that is then reacted with nitrobenzene to produce 3-bromobenzaldoxime. 3-Bromobenzaldoxime has been used in the synthesis of hydroxamic acids and its use as a solvent for nitro compounds.

4-Diethylaminobenzaldoxime is a reaction component that is used in the synthesis of complex compounds. It has been shown to be a useful scaffold for the construction of novel chemical entities. It also has high quality, and can be used as a reagent in research or as a speciality chemical. 4-Diethylaminobenzaldoxime is versatile and can be used as an intermediate or building block in organic chemistry. This chemical has CAS No. 54376-65-7 and is classified as a fine chemical.

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.

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.

(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%.

9-Fluorenone oxime is a pharmacological agent that has been shown to inhibit the activity of proteases. It has been shown to be effective in the treatment of hepatitis caused by radiation and amines, such as fluorenone. 9-Fluorenone oxime binds to the hydroxyl group of the active site on the protease enzyme and forms a covalent bond with it. This prevents hydrolysis of substrate proteins and thus blocks protein synthesis. 9-Fluorenone oxime also has chelate ligand properties, which allow it to bind to metal ions, such as phosphotungstic acid or fluorescence probes, and form complexes. The thermal expansion property of 9-fluorenones can be used for thermometry in biochemistry research.