Aminas

O-(Tert-butyldimethylsilyl)hydroxylamine is a stereospecific, oxidized, insoluble, tautomeric hydroxamic acid. It is used as a reagent in organic synthesis to form lactams by reaction with hexamethylenetetramine. The compound can be prepared by treatment of hydroxylamine with diacetate in the presence of aluminium chloride. The product is an orange liquid that crystallizes from water, but is not soluble in most organic solvents.

<p>4-Aminoanisole is a solvent that is used in analytical chemistry. 4-Aminoanisole has been shown to be an optimum concentration for x-ray diffraction data, sodium carbonate, and trifluoroacetic acid. It has been shown to have a redox potential of -0.14 V vs. NHE at pH 7.4 and a hydrogen bonding interaction with co2 gas. 4-Aminoanisole is used as a solvent in analytical chemistry and is also found in rat liver microsomes where it may play a role in the metabolism of certain drugs through its ability to inhibit cytochrome P450 enzymes.</p>

9-(Benzylamino)-1,2,3,4-tetrahydroacridin-1-ol maleate is a cholinergic drug that is used for the treatment of inflammatory diseases. It inhibits phosphodiesterase activity and has been shown to be effective in clinical studies against a number of inflammatory diseases. This drug also has anti-inflammatory properties and can be used to treat acute inflammation. 9-(Benzylamino)-1,2,3,4-tetrahydroacridin-1-ol maleate is also conjugated with fatty acids and this formation helps to increase its bioavailability.

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N-Nitrosodicyclohexylamine (NDCA) is a chemical that is used as a corrosion inhibitor. The stability of NDCA in the environment has been studied extensively and found to be resistant to many conditions including heat, light, and pH. NDCA is absorbed by the skin or ingested and has been shown to cause genotoxic effects in human lymphocytes. The genotoxic potential of NDCA has also been demonstrated in V79 cells. NDCA reacts with amines to form an intermediate that spontaneously decomposes into nitrosamines, which are carcinogenic. This reaction mechanism was confirmed using analytical methods such as gas chromatography-mass spectrometry (GC-MS).

Please enquire for more information about [2-(5-Chloro-1H-indol-3-yl)-1-methylethyl]amine hydrochloride including the price, delivery time and more detailed product information at the technical inquiry form on this page

<p>Intermediate in the synthesis of anagliptin</p>

4-Amino-1,3-dimethyl-2,6-dioxo-5-nitrosopyrimidine is a monoclonal antibody that binds to cancer cells. It has been shown to be effective in the treatment of leukemia, Hodgkin's disease, and non-Hodgkin's lymphoma. The binding of 4-Amino-1,3-dimethyl-2,6-dioxo-5-nitrosopyrimidine to cancer cells is due to the formation of a coordination geometry between the copper complex and the nitrogen atoms on the amino group. This drug has been shown to inhibit tumor growth by blocking the synthesis of DNA and RNA, which are key components in cell division. 4AADNP also inhibits cancer cells' ability to uptake glucose by inhibiting cellular glucose transporters. The binding affinity of 4AADNP for cancer cells is higher than for normal cells because cancer cells have more receptors for this drug

Please enquire for more information about N-[3-Fluoro-4-[(methylamino)carbonyl]phenyl]-2-methylalanine including the price, delivery time and more detailed product information at the technical inquiry form on this page

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3-(1-Naphthyl)propyl]amine is an organic compound that is a colorless solid with a melting point of -118°C. It is soluble in water, methanol, and acetone. 3-(1-Naphthyl)propyl]amine forms acid when heated with concentrated hydrochloric acid. The reaction produces hydrogen chloride gas and benzoic acid as a byproduct. 3-(1-Naphthyl)propyl]amine also reacts with pyridine to produce carbamic acid and ammonia gas as a byproduct. This can be rationalized systematically by the loss of the amine group from the nitrogen atom of the amine molecule. Carbamic acid has two acidic protons on it which are stabilized by the carbonyl group on the other side of the molecule. 3-(1-Naphthyl)propyl]amine can also react with anions such as carbonate ions to form carbamate salts,

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Indene-1-methanamine is a drug that has been used for the treatment of neurologic disorders and is an ester of aliphatic hydrocarbons. It has been shown to have antidepressant effects in animal models, which may be due to its ability to bind to 5-HT1A receptors. Indene-1-methanamine also has antimicrobial properties and can be used for treating bladder infections as well as cancer. This drug binds to the quinolizine site on bacterial DNA gyrase, which inhibits DNA synthesis and leads to cell death.

Nomega-Methyl-5-hydroxytryptamine oxalate salt is a drug that belongs to the group of serotonergic drugs. It is used as an antidepressant, and is also used for the treatment of Parkinson's disease. Nomega-Methyl-5-hydroxytryptamine oxalate salt acts by inhibiting the synthesis of serotonin in the brain. This drug can be taken in tablet form or orally dissolved under the tongue (sublingually). The therapeutic effects are observed after 1–2 weeks. Nomega-Methyl-5-hydroxytryptamine oxalate salt has been prospectively evaluated in clinical trials with various populations and shown to be effective in treating depression and Parkinson's disease.

<p>Please enquire for more information about 4-Amino-2-methylphenylboronic acid, pinacol ester including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

Cyclohexamine hydrochloride is a potent non-selective muscarinic antagonist that has been used as an anesthetic for rodents for the past three decades. It binds to the muscarinic acetylcholine receptors and blocks the effects of acetylcholine, which are involved in regulating heart rate, blood pressure, and other cardiovascular functions. It is also used to treat Alzheimer's disease by blocking acetylcholine from binding to its receptor. Cyclohexamine hydrochloride can cause psychotic symptoms such as hallucinations and delusions when taken in high doses. It may also be toxic to the cerebral cortex when administered at high doses.

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<p>Tetrabutylammonium hexafluorophosphate is a chemical reagent that is used in organic synthesis. It is a strong Lewis acid that reacts with substrates to form adducts. Tetrabutylammonium hexafluorophosphate reacts with trifluoroacetic acid, ethylene diamine, and hydrogen fluoride to produce the salt tetrabutylammonium hexafluorophosphate dihydrate (TBAPF). The reaction proceeds through an ionic intermediate that involves the abstraction of a proton from the substrate by the tetrabutylammonium cation followed by nucleophilic attack on the anion by water. Tetrabutylammonium hexafluorophosphate dihydrate can be formed via this mechanism as well as through a simple salt metathesis reaction between TBAPF and sodium carbonate. This reagent has been shown to form crystals of good quality for</p>

<p>Silyl protecting group for alcohols; reagent for introducing protected C atom</p>