Amines

Phthalazin-5-amine is an ionic liquid that is synthesised by the reaction of ammonium nitrate, pyridazine and formaldehyde. It has been used for the elucidation of hydrogenation reactions, desorption of organic compounds from silica gel, as well as for the synthesis of monomers. Phthalazin-5-amine also has a high reactivity with aldehydes, which can be used in reactive coupling reactions. The molecular weight was determined by mass spectrometry to be 222.14 g/mol. The compound is a white solid at room temperature and can be stored below -20°C.

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5-Carbomethoxytryptamine hydrochloride is a chemical building block that can be used as a reaction component for organic synthesis. It is a versatile intermediate and can be used in the production of fine chemicals, such as pharmaceuticals, dyestuffs, and pesticides. 5-Carbomethoxytryptamine hydrochloride is also an important reagent in both organic synthesis and analytical chemistry. The compound belongs to the group of indole alkaloids, which are found in plants of the Apocynaceae family. CAS No.: 74884-81-4.

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2’-Amino-2’-deoxy-β-D-arabinouridine is a modified nucleoside based on uridine, in which the 2'-hydroxyl group of the sugar has been replaced with an amino group, and the sugar itself is arabinose (a stereoisomer of ribose). This compound is of possible interest in nucleic acid chemistry and antisense or RNA-interference research.

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2-Amino-N-isopropylbenzamide is an amide compound that has been used as a pesticide. It has been shown to inhibit the activity of activated chloride channels in rat neutrophils and in cultured human erythrocytes, which leads to cellular hyperpolarization. 2-Amino-N-isopropylbenzamide also inhibits the release of protocatechuic acid from human neutrophils, which has been implicated in their activation and inflammatory response. This compound may be useful for the treatment of diseases such as meningitis and cranial cavity infections due to its ability to inhibit bacterial growth.

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N-(2-Aminoethyl)piperazine (NAPE) is a chemical compound that can be used as an environmentally friendly catalyst for the degradation of ethylene diamine and other amines. NAPE has been shown to be stable under alkaline conditions, and its fluorescence probe has been used to monitor the progress of the reaction. This compound is a coordination complex with nitrogen atoms at the corners of a square and two amines at opposite corners of the square. The amine groups are coordinated to metal ions in a geometry that is determined by the atomic number of the metal ion. Disulfide bonds form between two cysteine residues on adjacent chains. Glycol ethers can also form disulfide bonds with NAPE, forming glycol ether-NAPE complexes. Antibodies have been shown to bind to glycol ether-NAPE complexes, suggesting that these complexes may play a role in antibody response, although experimental solubility data have not yet confirmed this

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