Aminas

Please enquire for more information about 2-(((2,5-dimethoxyphenyl)sulfonyl)amino)benzamide including the price, delivery time and more detailed product information at the technical inquiry form on this page

Please enquire for more information about Ethyl 2-(4-(4-(trifluoromethyl)phenylamino)-3,5-thiazolyl)acetate including the price, delivery time and more detailed product information at the technical inquiry form on this page

The preparation of racemic N,N'-Bis(3,5-di-tert-butylsalicylidene)-1,2-cyclohexanediaminomanganese(III) chloride (S,S)-(+)-N,N'-Bis(3,5-di-tert-butylsalicylidene)-1,2-cyclohexanediaminomanganese(III) chloride is carried out by the reaction of salicyaldehyde with manganese dioxide in acetonitrile. The mixture is heated to reflux for 3 hours. The product is purified by recrystallization from hot acetonitrile and then purified again by preparative thin layer chromatography using a chiral stationary phase. The product is obtained as a white powder in an overall yield of 52%.
The synthesis of (R)-(-)-N-(3,5-Di-tert-butylsalicyl

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.

N-[3-(3-Dimethylamino-1-oxo-2-propenyl)phenyl]-N-ethylacetamide is a high quality, complex compound that is useful as a reagent, intermediate, and building block. The CAS number for this product is 96605-66-2. This product has shown to have use in the synthesis of fine chemicals and research chemicals. It is a versatile building block that can be used as a reaction component.

Dimethyldioctadecylammonium bromide is a cationic surfactant that is used as an antimicrobial agent. It has been shown to be effective against gram-positive and gram-negative bacteria and fungi. Dimethyldioctadecylammonium bromide also has the ability to bind to human immunoglobulin, which may be due to its disulfide bond structure. This surfactant has been shown to have biological properties in a model system, including optimum concentration and thermal expansion. The surface glycoprotein of the bacterium Pseudomonas aeruginosa is not affected by this surfactant, but it does show preferential binding for the protein that coats Staphylococcus aureus

2-Amino-4-bromobenzoic acid is a molecule that has an acidic carboxylic group and two aromatic amino groups. It has a hydroxyl group and a fluorescence that can be activated or deactivated by ultraviolet light. 2-Amino-4-bromobenzoic acid is used in the synthesis of certain organic compounds. This molecule can be synthesized from other molecules, such as phenol, aminobenzene, and nitrobenzene. The reaction time for this chemical species is dependent on the catalytic agent used during the reaction process. A variety of chemical species are produced when 2-Amino-4-bromobenzoic acid is synthesized, including hydrogen bromide, ammonia, nitrogen gas, and water vapor. The population of 2-Amino-4-bromobenzoic acid is unknown because it is not abundant in nature.

5-Aminoquinoline (5-AQ) is a chemical compound that was originally synthesized in the 1930s. 5-AQ is a trifluoroacetic acid derivative of quinoline, which has been used as a photographic developer and an agent for the removal of silver from photographic film. This molecule also has a fluorescence property, which can be seen when irradiated by light with a wavelength greater than 350 nm. A hydrogen bond exists between the hydroxyl group and the nitrogen atom of the amine group in 5-AQ. The reaction mechanism for 5-AQ is believed to involve the diazonium salt intermediate, which reacts with silver ions to form silver diazonide and free ammonia.
5-AQ is insoluble in water but soluble in organic solvents such as acetone or alcohol. It reacts with trifluoroacetic acid to form a precipitate, which may be removed by filt

2-Amino-3-chlorobenzonitrile is a linker in the synthesis of serotonin, an endogenous neurotransmitter that is involved in many physiological and psychological processes. The x-ray crystallographic studies of this molecule revealed that it has a similar structure to the analogs used for anticancer activity and bioassays. This molecule has shown anticancer activity against tumor cell lines with high levels of serotonin production, such as colon cancer cells. It also shows anti-cancer effects by binding to cryptochrome and stabilizing its structure. 2-Amino-3-chlorobenzonitrile interacts with hydrogen bonding interactions.

5-Amino-1,3-dimethyl-1,3-dihydro-2H-benzimidazol-2-one dihydrochloride (5ADMB) is a high quality reagent that is used as a complex compound. It has been shown to be useful in the synthesis of various compounds and is a fine chemical that can be used as a building block. 5ADMB has also been shown to be an excellent scaffold for the synthesis of benzo[b]thiophenes. This compound is also useful as a research chemical or specialty chemical. 5ADMB can be used in organic syntheses as a versatile building block and it reacts with nucleophiles such as alcohols and amines to form substituted derivatives. It has an appearance of white solid powder and its CAS number is 1986846-08-5.

DL-3-Aminoisobutyric acid (LAA) is a metabolite of the amino acid L-arginine. It is produced in the liver by the enzyme arginase and can be used to diagnose hepatic steatosis. It is also found in urine and human serum, as well as in microbial metabolism. LAA has been shown to regulate gene transcription and metabolism through its ability to inhibit the activity of gamma-aminobutyric acid (GABA), an inhibitory neurotransmitter that regulates energy metabolism and metabolic disorders. In addition, LAA has been shown to have antioxidant properties, which may be related to its role in caproic acid biosynthesis.

Methyl 4-aminocinnamate is an inhibitor of the integrase enzyme. It inhibits HIV-1 integrase and has been shown to be selective for this enzyme over other cellular enzymes. Methyl 4-aminocinnamate has been shown to inhibit cervical carcinoma, breast carcinoma, and esters as well as inhibiting the growth of human cancer cells in culture. The IC50 for methyl 4-aminocinnamate against cervical carcinoma was found to be in the micromolar range, which is considerably less than that of other anti-cancer agents.

Ammonium persulfate is used as a strong oxidizing agent in histological staining to produce an insoluble precipitate of silver sulfide on the tissue. It is also used for the manufacture of glycol ethers, which are solvents that are used in paints, varnishes, and lacquers. The reaction mechanism of ammonium persulfate is complex and involves three stages:
1) Ammonium persulfate reacts with water vapor to form hydrogen peroxide and ammonia gas.
2) Potassium dichromate reacts with hydrogen peroxide to form chromic acid and water.
3) The ammonium ion reacts with chromic acid to form a soluble salt (chromium(III) ammonium nitrate).
The reaction solution contains ammonium ions, which can be detected by electrochemical impedance spectroscopy (EIS).

Methyl 2-amino-3-bromobenzoate is a high quality, versatile building block that is used as a reagent and intermediate in the synthesis of biologically active compounds. Methyl 2-amino-3-bromobenzoate is a complex compound that has proven useful as an intermediate in the synthesis of various fine chemicals, such as speciality chemicals. The compound also serves as a useful scaffold for the preparation of other compounds, such as research chemicals. Methyl 2-amino-3-bromobenzoate can be used in reactions with other reagents to form new compounds. It is also used to make important reaction components, such as CAS No. 104670-74-8.

3-Methyl-5-isothiazolamine is a linear molecule with a molecular weight of 122.1. 3-Methyl-5-isothiazolamine has an interaction with chloride and can be used as a reagent for the identification of disulfides. Disulfide bonds are formed by the oxidation of sulfhydryl groups in proteins, which are reduced by glutathione reductase to produce sulfhydryl groups. 3-Methyl-5-isothiazolamine has been shown to react with molecular ions that are characteristic of isothiazoles and isothiazole derivatives, as well as aromatic compounds such as 4-hydroxybenzoic acid. This product also reacts with dehydrogenase enzymes, such as alcohol dehydrogenase, which produces oxidized products from carbohydrates and other organic molecules that contain hydroxyl groups.

Please enquire for more information about Ethyl 3-((4-chlorophenyl)amino)-5-methyl-2,4-thiazolecarboxylate including the price, delivery time and more detailed product information at the technical inquiry form on this page

2,5,6-Triaminopyrimidin-4-ol sulphate is a fine chemical that is used as a reagent in the synthesis of other compounds. It can be used as a building block for research chemicals and speciality chemicals such as pesticides. This compound is also useful in the manufacture of pharmaceuticals and agrochemicals. 2,5,6-Triaminopyrimidin-4-ol sulphate has been shown to react with aniline derivatives to produce a variety of products including pyrrolidine and piperidine derivatives. This versatile compound can also be used as a scaffold in the synthesis of complex molecules.

8-Aza-2,6-diaminopurine sulfate (1:x) is a sulfate salt that is soluble in water. The molecular mass of the compound is 581.10 g/mol and it has a molecular formula of C5H7N3O4S. The crystal structure of the compound consists of an asymmetric unit containing one molecule. The 8-aza-2,6-diaminopurine monohydrate salt has a solubility of 1 g/100 mL in water at 25°C. It also has a melting point of 190°C and a boiling point of 340°C.

Bis-Boc-amino-oxyacetic acid is an analog of goserelin acetate. It binds to the androgen receptor in prostate cancer cells, which leads to cytostatic effects. This drug has shown a low potency in human serum and does not bind to human serum proteins.
The uptake of Bis-Boc-amino-oxyacetic acid by prostate cancer cells was found to be significantly greater than that of goserelin acetate. The binding affinity of this drug for the androgen receptor is also lower than that of goserelin acetate, making it more selective for prostate cancer cells over other tissues.

(S)-(-)-3-Aminoquinuclidine 2HCl is a cholinergic agonist that has been shown to be effective in inducing the release of acetylcholine from brain synaptosomes. This drug binds to the nicotinic acetylcholine receptor (nAChR) and inhibits the action of the enzyme acetylcholinesterase, thereby increasing the concentration of acetylcholine in the synaptic cleft. The drug is also able to cross the blood-brain barrier and bind to receptors on neurons. It has been shown that this drug can be used as an imaging agent for molecular magnetic resonance tomography (MRT), with high sensitivity and specificity.

2-Amino-6-bromo-3-formylchromone is a chemical compound with the molecular formula CHNO. It has a vibrational frequency of 1426.81 cm−1 and a potential energy of −29.35 kcal/mol. The molecule can be classified as an aromatic compound, due to the presence of one or more benzene rings in its structure, and is colored red or orange in solution. 2-Amino-6-bromo-3-formylchromone can be used to produce other compounds that have different spectral properties than it does, such as 2-(2-(2-(2-(2-(2-(benzoyloxy)ethoxy)ethoxy)ethoxy)ethoxy)ethoxy)-4'-nitroacetophenone.

4-Amino-1-Boc-piperidine is a potent inhibitor of the CCR5 receptor. It is an x-ray crystal structure with a hydroxide solution that inhibits the growth of cancer cells. The inhibitor binding site for 4-Amino-1-Boc-piperidine was determined to be the CCR5 receptor, which is located on the surface of hematopoietic cells. The compound has been shown to inhibit human T lymphocyte proliferation in vitro and inhibit HIV replication in infected patients. 4-Amino-1-Boc-piperidine is able to inhibit the growth of cancer cells by blocking the production of cytokines, such as interleukin 2, that are needed for cell division and growth.