Building Blocks

<p>1-Bicyclo[4.2.0]octa-1,3,5-trien-7-ylmethanamine is an antitussive drug that acts as a radical and analgesic by binding to the opioid receptors in cells. 1-Bicyclo[4.2.0]octa-1,3,5-trien-7-ylmethanamine has been shown to have antitussive effects in animal models with no observable side effects on the central nervous system and cardiovascular system. The identity of this compound has not yet been confirmed.END&gt;</p>

<p>Versatile small molecule scaffold</p>

<p>2-(Bromomethyl)naphthalene is a chemical that has been studied extensively for its ability to inhibit the growth of cancer cells. It binds with high affinity to the mitochondrial membrane potential and inhibits the production of ATP, leading to cell death. 2-(Bromomethyl)naphthalene has also been shown to produce reactive oxygen species (ROS), which can also induce tumor cell death. This compound has been used in a variety of biological samples, including urine samples, which have shown promising results. A potential target for this drug is an enzyme called hydrolysis, which may be found at higher concentrations in tumor cells. The proposed reaction mechanism is shown below: 2- (bromomethyl) naphthalene + H 2 O → bromide ion + 2- (hydroxymethyl) naphthalene The kinetic data and diphenyl sulfoxide are unknown at this time.</p>

<p>N-Aminopyridine-2-carboximidamide (NAP) is a potent inhibitor of the β-catenin pathway. It is used to treat autoimmune diseases and cancer. NAP inhibits the activity of amidrazone, which is an inhibitor of the β-catenin pathway in mammalian cells. NAP has been shown to inhibit tumor growth and increase survival rates in mice with cancer. NAP also inhibits chloride channels, leading to hyperpolarization of human erythrocytes, which may contribute to its anti-inflammatory activity.</p>

<p>Methyl 3-methylisoxazole-5-carboxylate is an organic compound that belongs to the aldoxime class. It is used as a reagent in organic synthesis and as an intermediate in the synthesis of other compounds. Methyl 3-methylisoxazole-5-carboxylate can be prepared by the reaction of methyl chloroformate and 3-methylisoxazol-5-one. This compound reacts with nitrite to form hypochlorite, which can be used as a bleach or disinfectant. Methyl 3-methylisoxazole-5-carboxylate also reacts with amides, nitriles, and oxides to give tertiary amines and oximes respectively. The reaction system can be further modified by bromination or oxidation to give bromomethyl or methyl isoxazolines respectively.</p>

<p>Bromoacetaldehyde diethyl acetal (BDAE) is an organic compound that has been shown to have receptor binding activity. BDAE binds to the ethylene diamine receptor and competes with ethylene diamine for binding sites. It also forms acid from sodium carbonate and hydrochloric acid, which may be due to its ability to act as a solid catalyst. BDAE has shown activity in hiv infection, with a potency comparable to that of dimethyl fumarate. The synthesis of BDAE can be accomplished by reacting monosodium malonate ester hydrochloride with adenine nucleotide and malonic acid. The reaction solution is heated until the desired product crystallizes out of solution.</p>

<p>Bis[2-(perfluorooctyl)ethyl] phosphate is a perfluorinated compound that can be used as an alternative to polyvinyl chloride in the manufacture of children's toys and other consumer products. It has been shown to have no health effects on humans, unlike other perfluorinated compounds, in a study where human serum was analyzed. Bis[2-(perfluorooctyl)ethyl] phosphate also has a high affinity for polyfluoroalkyl substances (PFASs) and can be used in analytical methods for their detection. The optimised extraction procedure is simple and rapid, using ultrasonic extraction with no need for any organic solvents. Recoveries are high (&gt;99%) and the method does not require any volatile solvents.</p>

<p>Bis[(pinacolato)boryl]methane is a bifunctional organoboron reagent with an allyl group on one end and a cyclopropane on the other end. It is useful in organic synthesis as a nucleophile for allylation, as well as for the synthesis of unsymmetrical cyclopropanes. This compound can be used to catalyze asymmetric methods, such as the synthesis of alicyclic compounds. Bis[(pinacolato)boryl]methane can also be used to synthesize biomolecules.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Please enquire for more information about 5-Bromo-1-methyl-1H-1,2,3-triazole including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Please enquire for more information about 5-Bromo-oxazole-2-carboxylic acid methyl ester including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>2,6-Dimethyl-4H-pyran-4-thione is a ligand that binds to metal ions and forms coordination complexes. It has been shown to be an effective catalyst for the oxidation of alcohols and amines with molecular oxygen. 2,6-Dimethyl-4H-pyran-4-thione can also be used in the synthesis of organic compounds by reacting with halides. The optical and vibrational spectra are linear at low temperatures and exponentially increase at higher temperatures. This compound can be crystallized by XRD or fluorescence methods, depending on the desired outcome. Solvents such as acetone, NMP, DMSO, THF, water, and chloroform have been shown to affect the crystal structure of this compound in varying degrees.</p>

<p>Bromobenzene-d5 is a chemical compound that can be used as a chemical reagent for the production of other chemicals. It has a molecular weight of 188.21 and a melting point of -100°C. Bromobenzene-d5 has shown to be reactive with chloride and tert-butyl isocyanate, which are both strong bases. The molecule has an amorphous nature and exhibits vibrational properties at high frequencies. Bromobenzene-d5 also shows polarizability in the intramolecular hydrogen bond region, which is evident by an NMR spectrum of heterocycle bromobenzene-d5.</p>

<p>(4-Methylenecyclohexyl)methanol is a high-boiling liquid that is used as a solvent for various organic reactions. It is prepared by the oxymercuration of 4-methylcyclohexanol in the presence of tert-butyl alcohol and borohydride. The reaction proceeds with the formation of tert-butyl (4-methylenecyclohexyl) ether, which is hydrolyzed to give (4-methylenecyclohexyl)methanol. This intermediate can be further reduced with borohydride to yield tert-butyl alcohol.</p>

<p>4-Aminomethyl-phenol hydrochloride is a chemical compound that belongs to the group of amines. It is a white solid with a melting point of 126 °C and can be found in 5-ht7 receptor binding studies. 4-Aminomethyl-phenol hydrochloride has been shown to have an inhibitory effect on the dopamine receptors, which are involved in the regulation of movement and emotions. The inhibition of these receptors leads to decreased heart rate and blood pressure, as well as other symptoms such as nausea and vomiting. 4-Aminomethyl-phenol hydrochloride has also been shown to be a natriuretic agent, which reduces the concentration of sodium ions in urine by inhibiting the reabsorption of sodium ions from the kidney tubules. This drug is used for the treatment of high blood pressure.END&gt;</p>

<p>3-Cyano-1-methylpyridin-1-ium iodide is a reactive chemical that can be used as an electrophilic reagent. It reacts with amines, anilines, and pyridones to produce N-substituted pyridinium salts. 3-Cyano-1-methylpyridin-1-ium iodide also reacts with chloride ions to form the corresponding chlorides. This compound has been used in the synthesis of nucleophilic attack products such as benzyl bromide and phenylacetaldehyde.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>3-Bromothiophene is a homogeneous catalyst that can be used in organic synthesis. It has been shown to convert all-trans retinoic acid into 9-cis,11-trans retinoic acid. This conversion occurs through nucleophilic attack of the bromide ion on the carbon atom adjacent to the double bond in the carboxyl group of all-trans retinoic acid. 3-Bromothiophene has also been shown to have light emission properties in polymer films and metal halides.</p>

<p>Versatile small molecule scaffold</p>

<p>4,7-Dihydro-2,2-dimethyl-1,3-dioxepin is a cyclopropane. It has been used as a model substrate for the study of carbene mechanisms. The cyclopropanation of 4,7-dihydro-2,2-dimethyl-1,3-dioxepin is catalyzed by a metal carbene complex. The reaction mechanism and energetics have been studied in detail using dimethyl diazomalonate as the substrate.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>2,2-Bis(chloromethyl)oxirane is a chemical intermediate that can be used as a binder in the production of polyurethane and polyester resins. It can also be used to produce target products such as hydroxyethyl acrylate, methacrylic acid, and acrylic acid esters. 2,2-Bis(chloromethyl)oxirane is usually prepared by reacting methylene chloride with chloromethyl methyl ether in the presence of a catalyst such as tetrabutylammonium. The reaction mixture is heated to reflux for at least one hour before cooling to room temperature and adding an excess of water to quench the reaction.</p>

<p>Versatile small molecule scaffold</p>

<p>(S)-tert-Butyl 3-(methylamino)pyrrolidine-1-carboxylate is a research chemical that can be used as a versatile building block for the synthesis of complex compounds. It is also a reaction component in the synthesis of speciality chemicals and useful scaffolds. It has been shown to have high quality, reagent grade and purity.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>3-Bromo-5-phenyl-1,2,4-oxadiazole (3BrO) is an organic compound that can be synthesized by coupling a benzoyl chloride with a cyanide salt. 3BrO is also produced in the pyrolysis of benzophenone and 1,2,4-triazole. The fragmentation of 3BrO produces catechol and phenylhydrazine. The deoxygenative coupling reaction of 3BrO with sodium azide produces the explosive compound 2,4,6-trinitrobenzamide. This chemical has been used as the starting material for the synthesis of many other explosives such as RDX and TNT.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>2-Butynoic acid is a trifluoroacetic acid derivative that has been shown to inhibit the production of cytokines and inflammatory mediators in human macrophages. It has been used as a model system for studying the effects of alkanoic acids on antibody production. This drug may also be useful in treating autoimmune diseases by inhibiting the formation of antibodies. 2-Butynoic acid is an α-subunit inhibitor that prevents cellular transformation and tumor growth by preventing proliferation and metastasis. The drug inhibits the formation of disulfide bonds, which are essential for protein folding and function. 2-Butynoic acid has also shown synergistic effects with other drugs such as doxorubicin or hydrogen fluoride, which may lead to a more effective treatment for cancerous cells.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Please enquire for more information about 5-Bromo-2,3-dihydrobenzo[b]furan including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>2-Bromo-6-hydroxybenzaldehyde is a synthetic chemical that consists of a furan ring with an acetonitrile group. It has been shown to be a constant in cyclic electroreduction and is used as a biomolecular surfactant. 2-Bromo-6-hydroxybenzaldehyde has also been shown to react intramolecularly with the hydroxyl group on the benzene ring, which results in the formation of a dimer. This chemical can be produced by solvolysis or electroreduction.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>6-Bromopyridine-3-carboxaldehyde (6-BPAR) is a synthetic compound that binds to copper ions and has been shown to have inhibitory activities against trifluoroacetic acid, calcium carbonate, optical properties, and low energy. 6-BPAR also has an aldehyde group and hydroxamic acid group. This chemical can be used as a catalyst for the hydrogenation reduction of metal ions such as chloride or formyl groups.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>