Iminas

<p>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</p>

<p>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</p>

<p>2,4-Dimethoxybenzaldoxime is an aldoxime that has been used in the synthesis of formyl compounds. It is a synthetic molecule with a molecular weight of 192.2 g/mol and a melting point of 97°C. 2,4-Dimethoxybenzaldoxime is used to synthesize fulvenes, which are highly reactive molecules that have been shown to be useful in the study of formyl group reactivity. It also has been used as a photosensitizer for photochemical reactions. In addition, it can be used to prepare unsaturated alkyl compounds by reacting with alcohols in the presence of base or acid.</p>

<p>Benzenesulphonyl)acetamide oxime is a herbicide that inhibits the growth of plants by binding to the enzyme acetohydroxy acid synthase, which is involved in the synthesis of fatty acids. The compound has been shown to be a potent herbicide against many types of weeds, such as thistles, canary grass, ragweed, and lambsquarters. Benzenesulphonyl)acetamide oxime is also used as an analytical reagent to detect peroxides.</p>

<p>Please enquire for more information about 4-Bromobenzenesulphonylacetamide oxime including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>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.<br> Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package<br>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<br></p>

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

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

<p>Applications Butyraldoxime (cas# 110-69-0) is a useful research chemical.<br></p>

<p>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.<br>References Imamoto, T. et al.: J. Am. Chem. Soc., 112, 5244 (1990); Augeri, D. et al.: J. Med. Chem., 48, 5025 (2005);<br></p>

<p>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.<br>References Guinchard, X. et al.: J. Org. Chem., 73, 2028 (2008)<br></p>

<p>Applications Deoxybenzoin Oxime (cas# 26306-06-9) is a compound useful in organic synthesis.<br></p>

<p>Applications A degradation product of herbicide Molinate in pot soil and rice plants.<br>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),<br></p>

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

<p>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.<br>References Guinchard, X. et al.: J. Org. Chem., 73, 2028 (2008)<br></p>

<p>50% in water; Average molecular weight 800 Da</p>

<p>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</p>

<p>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</p>

<p>Testosterone 3-(O-carboxymethyl)oxime is an inactive prodrug of testosterone. It is a potent and selective inhibitor of angiotensin II that causes vasodilation by blocking the conversion of angiotensin I to angiotensin II. Testosterone 3-(O-carboxymethyl)oxime has been shown to be effective in lowering blood pressure in patients with congestive heart failure, although it may cause side effects such as dizziness, headache, and nausea. This drug can also be used to treat prostate cancer because it inhibits the production of testosterone and reduces serum levels of luteinizing hormone. Testosterone 3-(O-carboxymethyl)oxime can also be used for diagnostic purposes as a marker for polycystic ovary syndrome (PCOS).</p>

<p>Descarbamoyl cefuroxime is a prodrug that is hydrolyzed in vivo to cefuroxime, its active form. It can be prepared by acylation of cefuroxime with an organic acid chloride, such as acetyl chloride or propionyl chloride. The reaction is catalyzed by a strong base, such as sodium hydride or potassium tert-butoxide. Descarbamoyl cefuroxime has been shown to be effective against Staphylococcus aureus and Clostridium perfringens, although is not active against acid-fast bacteria such as Mycobacterium tuberculosis or Mycobacterium avium complex. This drug has shown anti-inflammatory properties, which may be due to its inhibition of prostaglandin synthesis.</p>

<p>L-Buthionine-(S,R)-sulfoximine (BSO) is a glutathione-depleting agent that causes cell death by interrupting mitochondrial functions. BSO has been shown to be reactive with covalent linkages in polymer compositions and enzyme activities, which results in the inhibition of human osteosarcoma cells. It also has pro-apoptotic properties that have been demonstrated using multivariate logistic regression on taxol toxicity studies. Resistance to BSO is rare, but has been observed in breast cancer cells. The synergistic effect of BSO and other drugs, such as chemotherapeutic agents, is not well understood.</p>

<p>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.</p>

<p>(Z)-1-(2,4-Dichlorophenyl)-2-(1H-imidazol-1-yl)ethanone oxime is an antifungal agent that inhibits the synthesis of ergosterol, a major constituent of fungal cell membranes. It has been shown to be active against a variety of fungi and yeasts. (Z)-1-(2,4-Dichlorophenyl)-2-(1H-imidazol-1-yl)ethanone oxime also has antimicrobial activity against bacteria such as Staphylococcus aureus and Pseudomonas aeruginosa.</p>

<p>The heterocycle alpha-chloro-2-nitrobenzaldoxime is a functional group that can be oriented in two different ways. The diversity of the product arises from the fact that it is possible to create new functional groups by substitution on the benzene ring and on the nitrogen. Heterocyclization of alpha-chloro-2-nitrobenzaldoxime can be achieved by using other heterocycles such as isoxazoles, which are readily available in large quantities, as building blocks. This reaction can be catalyzed by reductive means with sodium borohydride and methanol.</p>

<p>Please enquire for more information about alpha,3-Dichlorobenzaldoxime including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>