Imines

Applications A degradation product of herbicide Molinate in pot soil and rice plants.
References Kriek, E., et al.: Biochemistry, 6, 177 (1967), Farmer, P., et al.: Toxicol. Lett., 149, 3 (2004), Gyorffy, E., et al.: Carcinogenesis, 25, 1201 (2004),

Applications Cyclopentanimine can be obtained from Cyclopentanone (C988395) which is a chemical compound used in the synthesis of various simple and complex organic compounds. Also used in the synthesis of peptidase IV inhibitors for the treatment of type 2 diabetes.
References Imamoto, T. et al.: J. Am. Chem. Soc., 112, 5244 (1990); Augeri, D. et al.: J. Med. Chem., 48, 5025 (2005);

Applications (E)-1-(Benzo[b]​thiophen-​2-​yl)ethanone Oxime is an isomer of N-​(1-​Benzo[b]​thiophen-​2-​yl-​ethyl)​-​hydroxylamine a reagent used in the preparation of Zileuton, an anti-asthmatic drug.
References Guinchard, X. et al.: J. Org. Chem., 73, 2028 (2008)

Applications Deoxybenzoin Oxime (cas# 26306-06-9) is a compound useful in organic synthesis.

Applications (Z)-1-(Benzo[b]​thiophen-​2-​yl)ethanone Oxime is an isomer of N-​(1-​Benzo[b]​thiophen-​2-​yl-​ethyl)​-​hydroxylamine a reagent used in the preparation of Zileuton, an anti-asthmatic drug.
References Guinchard, X. et al.: J. Org. Chem., 73, 2028 (2008)

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

Applications An antioxidant
References Jeong, H., et al.: Bioorg. Med. Chem. Lett., 16, 5576 (2006), Andresen Bergstroem, M., et al.: J. Med. Chem., 51, 2541 (2008),

Applications 9,10-Dihydro-1-benzo[a]pyrene-7(8H)-one Oxime (cas# 88909-82-4) is a compound useful in organic synthesis.

Applications (E)-1-(2,6-Dimethylphenoxy)propan-2-one oxime is a useful reagent for organic synthesis.

Applications Butyraldoxime (cas# 110-69-0) is a useful research chemical.

Please enquire for more information about O-(2,3,4,5,6-Pentafluorobenzyl)formaldoxime including the price, delivery time and more detailed product information at the technical inquiry form on this page

4-Fluorobenzaldehyde oxime is a phenylhydrazine derivative that reacts with an aromatic amine to form a ternary complex. The reaction time for this process is short, and the yield of the product is high. 4-Fluorobenzaldehyde oxime also reacts with an aromatic amine to form an ion-pair. It can react with acidic hydrogen donors such as peracids and it also has high hydrogen bonding interactions. 4-Fluorobenzaldehyde oxime is used in pharmacological agents as well as other chemical reactions, including halogenation.

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.

Deoxybenzoic oxime is an oxime derivative that inhibits the enzyme toll-like receptor 4 (TLR4) and also blocks activation of chloride channels. It has been shown to inhibit the production of nitric oxide and proinflammatory cytokines in vitro. Deoxybenzoic oxime has also been shown to have a broad spectrum of activity against chemical species, such as benzonitrile, sulfide, and amines. This drug has shown inhibitory activities against a wide variety of functional groups including hydroxyl, nitrile, amine, thiol, ethers, phosphates and carboxylic acids.

Please enquire for more information about 2,5-Dichlorobenzenesulphonylacetamide oxime including the price, delivery time and more detailed product information at the technical inquiry form on this page

Please enquire for more information about Naphthalene-2-sulphonylacetamide oxime including the price, delivery time and more detailed product information at the technical inquiry form on this page

Veratraldoxime is a synthetic compound that is the diacetate ester of oxime and has been used in the treatment of inflammatory bowel disease. It has been shown to be effective in some patients, but not all, with ulcerative colitis. Veratraldoxime inhibits the production of inflammatory mediators by inhibiting the activity of cyclooxygenase-2 and lipoxygenase. This drug also has anti-inflammatory properties by inhibiting prostaglandin synthesis at the level of phospholipase A2 and cyclooxygenase-1. The mechanism of action for this drug is similar to that of other nonsteroidal anti-inflammatory drugs (NSAIDs). Veratraldoxime also inhibits protein synthesis by blocking the formation of amide bonds, thereby inhibiting bacterial growth. The oxidation products are responsible for its antibiotic properties. Veratraldoxime binds to copper chromite to form a coordination complex, which is

Dimethylglyoxime is a chelate ligand that can be used as an antimicrobial agent. The compound binds to metals, such as iron and copper, which are found in wastewater and industrial effluents. Dimethylglyoxime can also chelate metal ions that are present in the water supply. This property makes it an effective agent for removing heavy metals from water. Dimethylglyoxime has been shown to react with various metal ions by means of Langmuir adsorption isotherms and fluorescence spectrometry. When this reaction occurs, the compound forms a complex with the metal ion. The model system is a solution of dimethylglyoxime with sodium citrate and tetramethylammonium chloride (TMA). The reaction mechanism involves protonation and deprotonation of the ligand, which occurs when the pH is changed from acidic to basic conditions. The plasma mass spectrometry technique has been used to detect the presence of dimethyl