Imines

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

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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 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).

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.

alpha,4-Dichlorobenzaldoxime is a synthetic ligand that inhibits bacterial DNA replication. It has been shown to inhibit the growth of staphylococcus and streptococcus by binding to their nucleic acids and preventing transcription. alpha,4-Dichlorobenzaldoxime may have anticancer potential and could be useful in chemotherapy treatments for some types of cancer. The mechanism of action is thought to be due to its ability to react with an amine group on an amino acid or protein, forming a hydroxyamine intermediate which can react with another amine group on another molecule. This reaction leads to the formation of a new chemical bond between the two molecules and prevents the production of proteins vital for cell division.

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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.

Applications Acetaldoxime is a useful research chemical, an intermediate or a precursor used in the preparation of some heterocyclic compounds like spiroisoxazolines. An oxygen scavenger in boiler water. 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 Lee, C. K. Y., et al.: ARKIVOC, 3, 175 (2006); Gallos, J. K., et al.: J. Chem. Soc., 4, 415 (2001); Zhao, Z., et al.: From Faming Zhuanli Shenqing (2019), CN 109368821 A 20190222

D,L-Buthionine-(S,R)-sulfoximine is a basic compound with a sulfur atom. It has been shown to have antioxidative properties. D,L-Buthionine-(S,R)-sulfoximine can be used in the treatment of infectious diseases caused by bacteria or viruses that are sensitive to oxidative injury. It also has inhibitory properties against toll-like receptor 4 (TLR4), which may be useful for treating inflammatory bowel disease. D,L-Buthionine-(S,R)-sulfoximine can also be used as an anti-inflammatory agent and an antioxidant in eye disorders. This compound can be used in the treatment of radiation injuries and eye disorders due to its ability to inhibit cell nuclei from dying by preventing DNA fragmentation.

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2,6-Dimethoxybenzaldoxime is a phenylhydrazone that can be used in the catalytic system for oxidation of carbonyl compounds. The reaction proceeds through the periodate-mediated oxidation of the hydrazone to form the corresponding hydroxamic acid. This compound has been shown to be efficient and selective for the oxidation of a wide range of carbonyl compounds, including porphyrins. 2,6-Dimethoxybenzaldoxime is also used as a precursor for other syntheses, such as tetraphenylporphyrin.

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