Amines

<p>RR,R)-(-)-N,N'-bis(3,5-di-tert-butylsalicylidene)-1,2-cyclohexanediamine is a coordination compound that is used as a catalyst in organic chemistry. It has been shown to catalyze the reaction of benzaldehyde with nitroethane to give phenylamine. RR,R)-(-)-N,N'-bis(3,5-di-tert-butylsalicylidene)-1,2-cyclohexanediamine also catalyzes the reaction of cyclohexanol with nitroethane to give phenylethylene. The selectivity of this catalyst depends on the site of adsorption and the ligand. This compound has been shown to be electrocatalytic by promoting the oxidation of anilines at a platinum electrode in water solution with an applied potential.</p>

<p>Please enquire for more information about 2-Bromobenzo[d]thiazol-6-amine including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

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<p>Fmoc-(3S,4S)-4-amino-3-hydroxy-6-methylheptanoic acid is a pharmacokinetic drug that is under investigation for prostate cancer. It has been shown to inhibit the growth of prostate carcinoma cells and reduce the expression of prostate specific antigen (PSA) in vivo. Fmoc-(3S,4S)-4-amino-3-hydroxy-6-methylheptanoic acid has also been used in bioconjugate chemistry to produce a prodrug that can be taken orally. This prodrug is activated by viral proteases in the stomach, leading to an increase in cytotoxicity against HIV virus and other retroviruses. Fmoc-(3S,4S)-4-amino-3-hydroxy-6-methylheptanoic acid has also been shown to inhibit the production of human serum erythropoietin (EPO).</p>

<p>N-Methoxymethyl-N-(trimethylsilylmethyl)benzylamine is a chiral, electron deficient reagent that reacts with aldehydes and boronic esters to form products with high chemical yields. This compound can be used as a catalyst for acylation reactions, such as the synthesis of p-nitrophenol. N-Methoxymethyl-N-(trimethylsilylmethyl)benzylamine is synthesized by the reaction of trifluoroacetic acid and an amine, followed by chloroformate displacement. The product is then reacted with acylating agents in the presence of catalysts.</p>

<p>(2-Furylmethyl)methylamine is a protein inhibitor that has been shown to inhibit γ-secretase, an enzyme responsible for the cleavage of amyloid precursor protein (APP) and the production of beta-amyloid. It has also been shown to be effective in treating cancer and Alzheimer's disease when administered as an intravenous injection or oral medication. The effects on animals were observed in a study involving mice with bladder cancer. (2-Furylmethyl)methylamine was found to inhibit the growth of bladder cancer cells and induce apoptosis. This compound also inhibits glycogen synthase kinase 3 (GSK3), which is involved in cell proliferation. Trichophyton mentagrophytes, a fungus that causes athlete's foot, has also been found to be sensitive to this drug. Heterocycles are not affected by this compound because they lack nitrogen atoms at their positions corresponding to those in the amide group</p>

<p>1,5-Diaminoanthraquinone (1,5-DA) is an intermolecular hydrogen bonding compound that has been used as an optical sensor. The 1,5-DA molecule has the ability to form hydrogen bonds with chloride and sodium carbonate. This interaction can be exploited for surface-enhanced Raman spectroscopy of cell nuclei. The 1,5-DA molecule also interacts with supramolecular assemblies to produce surface-enhanced Raman scattering. In addition, 1,5-DA has a metal chelate property that allows it to bind to ferrocene carboxylic acid molecules. It can also form hydrogen bonds with vinyl alcohol molecules in multiwall carbon nanotubes. The molecular structure of 1,5-DA consists of rings containing five carbons each. These rings are linked together by amine groups and are attached to a central nitrogen atom on one end and a hydroxyl group on the other end.</p>

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<p>2-Amino-6-fluorobenzoic acid ethyl ester is a chemical that can be used as a building block in the synthesis of more complex compounds. It is a versatile intermediate and can be used to synthesize other important compounds, such as pharmaceuticals. This compound has been shown to be useful for the preparation of 2-amino-4,6-difluorobenzoic acid ethyl ester and many other derivatives. The colorless solid is soluble in ether and dichloromethane.</p>

<p>5-Bromoquinolin-8-amine is a topoisomerase inhibitor that can be used as an antitumor agent. It has been shown to inhibit the growth of tumor cell lines and suppress the growth of colon carcinoma cells in rats and human colon carcinomas in mice. 5-Bromoquinolin-8-amine interacts with DNA, specifically inhibiting the formation of supercoiled DNA. This interaction may lead to the inhibition of tumor cell growth. 5-Bromoquinolin-8-amine also inhibits protein synthesis by interacting with proteins at the ribosomal level, leading to inhibited cell growth.</p>

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<p>4,4'-Diaminostilbene is a chemical compound that is stable in the presence of alkali metals. It also has been shown to be titrated with sodium salts and to have a cavity that can be analyzed by fluorescence. 4,4'-Diaminostilbene has been used for the detection of beta-cyclodextrin and sodium ion in analytical methods. The intensity of its fluorescence depends on the concentration of aniline and protonated amines. This compound has been used as a reagent for nmr spectroscopy analysis.</p>

<p>Tetrabutylammonium acetate is a complex of tetrabutylammonium with the trifluoroacetate anion. It has been used as a reagent for the preparation of α-hydroxylated ketones, including natural products. Tetrabutylammonium acetate can be used in titration calorimetry to measure the heat evolved during the reaction between hydroxyl group and sodium salts. The heat released corresponds to the amount of water produced from this reaction. In this way, it can be determined whether or not a molecule contains an active hydrogen atom. Tetrabutylammonium acetate also reacts with reactive compounds such as dpp-iv inhibitors, forming a reactive intermediate that cannot be isolated due to its instability. This intermediate is detected by analytical methods such as plasma mass spectrometry or infrared spectroscopy. Tetrabutylammonium acetate also reacts with asymmetric synthesis, forming an intram</p>

<p>3-Amino-2-methoxy-dibenzofuran (3AMD) is a cytotoxic agent that is used in the treatment of bladder carcinoma. 3AMD inhibits DNA synthesis, leading to cell death by inhibiting the production of proteins vital for cell division. 3AMD has been shown to be a potent inhibitor of cyclen-dependent kinases and to induce DNA damage in human cells. 3AMD also has significant cytotoxicity against malignant cells and has been shown to inhibit the growth of tumours in mice. 3AMD may have carcinogenic potential due to its structural similarity with other carcinogens such as aniline and aminobiphenyl.</p>

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<p>Tritylamine is an inorganic acid that is synthesized by the reaction of trifluoroacetic acid with ammonia. It can be used to treat autoimmune diseases, such as rheumatoid arthritis, and has been shown to have a beneficial effect on collagen synthesis. Tritylamine has also been studied as a fluorescent probe for the detection of metal ions in biological systems. Tritylamine has been used in asymmetric synthesis and can also inhibit enzymes that catalyze metabolic reactions.</p>

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<p>4-((5-Bromopyridin-2-yl)amino)-4-oxobutanoic acid (BABA) is a potent photosynthetic inhibitor that inhibits light-driven electron transport in chloroplasts. This inhibition of electron transport leads to the accumulation of reactive oxygen species and cellular dysfunction. BABA is used to induce dormancy in plants and is also used as a chemical inhibitor for arabidopsis thaliana, a type of plant commonly used in molecular biology research. Studies have shown that BABA inhibits the growth of fat cells, which may be due to its ability to inhibit protein synthesis, leading to decreased fat deposition. In addition, this drug has been shown to reduce eye disorders such as retinal degeneration and cataracts by inhibiting the production of reactive oxygen species, which causes oxidative stress.</p>

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