Amines

Please enquire for more information about (4-Trifluoromethyl-pyridin-3-yl)methylamine hydrochloride including the price, delivery time and more detailed product information at the technical inquiry form on this page

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Please enquire for more information about N-(2-Methyl-5-nitrophenyl)-4-(3-pyridinyl)-2-thiazolamineHydrobromide including the price, delivery time and more detailed product information at the technical inquiry form on this page

Please enquire for more information about [(5-Phenyl-1H-pyrazol-3-yl)methyl]amine including the price, delivery time and more detailed product information at the technical inquiry form on this page

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2-Amino-5-bromo-6-(2-fluorophenyl)-1H-pyrimidin-4-one is a drug that belongs to the pyrimidine derivative class. It has significant activity against cancer cells in vitro and in animals. 2ABP4 also has synergistic effects with other drugs, such as aniline and dimethylformamide, and can form solvates with long-chain alcohols. This compound is being developed for the treatment of cancer.

Ammonium carbonate is an inorganic salt that consists of ammonium ion and carbonate ion. It is a white crystalline solid with a molecular weight of about 166.4 g/mol. Ammonium carbonate is soluble in water, alcohol, acetone, and other organic solvents. It has been used as a buffer solution for pH adjustment and as a source of ammonium ions in analytical chemistry. Ammonium carbonate can be formed by the reaction of sodium carbonate with ammonia gas or liquid ammonia, or the reaction of sodium bicarbonate with ammonia gas or liquid ammonia. The thermal expansion coefficient of ammonium carbonate is higher than those of sodium salts such as sodium chloride and potassium chloride. Electrochemical impedance spectroscopy (EIS) measurements have shown that the reactivity between ammonium carbonate and plasma mass spectrometry is high due to its high values on the electric spectrum graph at low frequencies (1 kHz).

5-Benzyl-1,3,4-thiadiazol-2-amine is an isothiocyanate that has been synthesized. It has a crystallography profile that can be optimized and it binds to diacylglycerol with an inhibitory effect. 5-Benzyl-1,3,4-thiadiazol-2-amine inhibits the activity of hydroxamic acids and triazine herbicides. This compound also exhibits inhibitory effects on phosphatases and histone deacetylases in tissues and carcinoma cells.

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Ethyl 5-amino-1H-pyrazole-3-carboxylate is a potent agonist of the soluble guanylate cyclase enzyme that produces guanylate. It has been shown to be effective in hepatitis virus, and is thought to act by binding to the viral polymerase protein. This drug also binds to the rna polymerase enzyme, which is responsible for converting RNA into DNA. The affinity of ethyl 5-amino-1H-pyrazole-3-carboxylate for these enzymes is low and it has a low yield when synthesized enzymatically. However, this drug has been shown to be potent agonists at these enzymes, with an affinity that is greater than other drugs used against hepatitis viruses such as interferon

A condensation reaction between an aldehyde and a benzaldehyde in the presence of p-toluenesulfonic acid and mercaptoacetic acid yields 5-amino-1,3-diphenyl-1H-pyrazole. This reaction is efficient and produces a high yield, making it an efficient method for synthesizing this chemical. The product is an aromatic compound that belongs to the class of heterocyclic compounds with two nitrogen atoms. It is also the 3rd member of the pyrazole family.

Please enquire for more information about [3-(4-Methylpiperazin-1-yl)propyl](2-thienylmethyl)amine including the price, delivery time and more detailed product information at the technical inquiry form on this page

4-Fluorobenzene-1,2-diamine is a monomer that is used in the synthesis of pesticides. It has been shown to have antibacterial activity against Gram-positive bacteria such as Staphylococcus aureus and Bacillus cereus. 4-Fluorobenzene-1,2-diamine has functional groups that are susceptible to reaction with amines. The reaction time for this chemical compound is less than 10 hours under standard conditions. br>br> 4-Fluorobenzene-1,2-diamine can be synthesized by reacting chloroform with dimethylamine and protonating the resulting product with thionyl chloride. The chemical formula for 4-fluorobenzene-1,2-diamine is CHClN(CH) 2.br>br> The structural formula of 4-fluorobenzene 1,2

Please enquire for more information about Methyl 2-[(E)-2-(dimethylamino)vinyl]-5-oxo-6-(4H-1,2,4-triazol-4-yl)-5,6-dihydro-1,6-naphthyridine-3-carboxylate including the price, delivery time and more detailed product information at the technical inquiry form on this page

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