Pharmaceutical Standards

1-(3-Bromophenyl)-2-nitropropane is a fine chemical that is used as a building block in the synthesis of complex organic compounds. It can be used as a reagent and speciality chemical with high quality. 1-(3-Bromophenyl)-2-nitropropane is versatile for use in reactions, such as coupling reactions, because it can be used as an intermediate or scaffold to create many different compounds. CAS No.: 155988-18-4

3,4'-Dimethoxy-2'-hydroxychalcone is a reaction component and useful scaffold for the synthesis of complex compounds. This chemical is an intermediate in the synthesis of various pharmaceuticals, such as anti-tuberculosis drugs, cancer chemotherapeutics and antibiotics. 3,4'-Dimethoxy-2'-hydroxychalcone has been shown to be a versatile building block that can be used to synthesize both natural products and pharmaceuticals. This compound also has a wide range of applications in the production of fine chemicals.

2',4-Dihydroxy-3-methoxychalcone is a chalcone that has been shown to have reactive properties. The compound was found to be cytotoxic to cancer cells in the presence of neutrophils, and it has been shown to inhibit the growth of t47d cells in culture. There is also evidence that 2',4-Dihydroxy-3-methoxychalcone may help regulate the microflora in the gut, which may help prevent obesity and diabetes. In epidemiological studies, 2',4-Dihydroxy-3-methoxychalcone was found to be protective against cancer, but more research is required.

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Copper naphthenate is a cross-linking agent that contains copper and nitrogen atoms. It reacts with potassium dichromate, sodium carbonate, and other substances to form a copper complex. Copper naphthenate is used in the manufacture of biodiesel as a preservative. The product also has insecticidal properties, which have been shown to be due to its ability to inhibit the activity of chitin synthase enzymes found in insects. Copper naphthenate has been shown to be effective as a contraceptive when used vaginally and may also be used topically on the skin for this purpose. This product is acidic and should not be mixed with other acidic substances or materials such as plastics or rubber.

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Please enquire for more information about 2-amino-7-methyl-4-(2-naphthyl)-5-oxo-4,6,7,8-tetrahydro2H-chromene-3-carbonitrile including the price, delivery time and more detailed product information at the technical inquiry form on this page

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Camphorquinone-10-sulfonic acid hydrate is a soybean trypsin inhibitor that is used as a preparative agent in organic synthesis. It reacts with histidine, lysine residues, and other molecules to form a light-chain kinase that inhibits the action of the enzyme trypsin. Camphorquinone-10-sulfonic acid hydrate has been shown to be resistant to proteolysis by gastrointestinal enzymes. This agent also has diabetogenic properties by inhibiting the activity of membrane potential and chloride channels in pancreatic β cells. Camphorquinone-10-sulfonic acid hydrate forms an ion pair with choline, which can inhibit the enzyme acetylcholinesterase, leading to accumulation of acetylcholine at nerve endings.

1-(3-Chlorophenyl) thiourea is a curcumin analog that has been shown to inhibit the epidermal growth factor (EGF) receptor. It is synthesized from 1,2-dichlorobenzene and urea in a two-step process. The anhydrous potassium carbonate is first converted to the potassium salt with an acid chloride. The second step is the reaction of this salt with urea in the presence of excess anhydrous potassium carbonate. This product has been shown to be effective against cancer cells and may be used as a potential anticancer agent for treatment of skin cancer. 1-(3-Chlorophenyl) thiourea inhibits EGF receptor by binding to it and preventing its activation, which prevents cell proliferation and reduces tumor size.

N-(4-Fluorophenyl)thiourea (FPTU) is a molecule that belongs to the class of thioureas. It has been shown to have a constant dihedral angle and is membrane transportable, which may be due to its ability to bind receptor proteins. FPTU has also been shown to inhibit chloride ion transport through the intestinal wall. In addition, it has been shown to have anti-inflammatory properties in animal models, which may be due to its ability to inhibit γ-aminobutyric acid (GABA) synthesis.