Building Blocks

<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>

Versatile small molecule scaffold

<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>

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

<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>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>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>

3-Bromo-4H-1,2,4-triazole is a triazole that is soluble in water. It has been shown to be an effective inhibitor of the enzyme DNA gyrase at low temperatures (4 degrees Celsius). 3-Bromo-4H-1,2,4-triazole has been analysed by spectroscopic methods and found to possess vibrational and annular spectra. The tautomers of this substance are also known to exist.

<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>3-Bromoquinoline is a brominated quinoline derivative that can be synthesized by cross-coupling reactions. The compound's chemical structure is similar to the 3-azidoquinoline, which was studied in quantum theory and molecular modeling. The 3-bromoquinoline molecule has been shown to exist in two different coordination geometries: octahedral and trigonal bipyramidal. In the octahedral geometry, the 3-bromoquinoline molecule is bound to three bromine atoms and one nitrogen atom, with an intramolecular hydrogen bond between the nitrogen atom and the quinoline ring system. The trigonal bipyramidal geometry also features an intramolecular hydrogen bond between the nitrogen atom and quinoline ring system, as well as a halogen bonding interaction with one of the three bromine atoms.</p>

<p>Please enquire for more information about tert-Butyl azetidine-3-carboxylate 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 Benzydamine hydrochloride EP Impurity D including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>8-Bromoisoquinoline is a bifunctional alkylating agent that is used to synthesize esters and amides. It is commonly used for the synthesis of amino acids, peptides, and other biologically active molecules. 8-Bromoisoquinoline has been shown to have a synergistic effect with hydroxyalkyl carbamates, which may be due to its ability to form an ionic bond with the carboxylic acid in these compounds. This chemical can also react with nitro groups and serve as a chlorinating agent, as well as react with anions such as phosphate and acetate. 8-Bromoisoquinoline can be synthesized by reacting ethyl bromoacetate with tetrahydroisoquinolinium chloride in hydrochloric acid or isopropyl alcohol.</p>

<p>2-Bromo-1,3,5-triisopropylbenzene is an ethylene acetal that is prepared by the catalyzed reaction of aryl chlorides and anhydrous zinc bromide in the presence of triethylamine. The selectivities of this method are high because it can produce mainly a single isomer. The stereoselectivity is also high because the reaction proceeds with the formation of only one stereoisomer. The mechanism for this reaction involves a nucleophilic substitution of the halogenated aryl chloride with the trialkylborane, which generates two different products. This product has been used in the synthesis of biphenyls and nitro compounds.</p>

<p>Please enquire for more information about Boc-4-(4-fluorophenyl)-piperidine-4-carboxylic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>1-Bromo-2-fluoro-3-nitrobenzene is a synthetic chemical that is used as an intermediate in the synthesis of various dyes. It can be obtained by the diazotization of acetyl nitrite and acetonitrile, followed by acetylation with acetic anhydride and hydrolysis with sodium hydroxide. The bromoaniline formed after this reaction is then converted to 1-bromo-2-fluoro-3-nitrobenzene by refluxing it with nitric acid. This chemical can also be synthesized from bromines and chloride in the presence of a diazo salt. It reacts with fluoride or halogens to produce fluorobenzene derivatives, which are used as intermediates for other organic compounds.</p>

<p>4-Cyanobenzoic acid (4CB) is a benzene derivative that inhibits the activity of tyrosinase, an enzyme involved in the production of melanin. It is synthesized by reacting 2,4-dichlorobenzoic acid with sodium hydroxide and acetone. 4CB has been shown to have a potent inhibitory effect on the enzyme, with an isolated yield of up to 83%. The compound also shows strong hydrogen bonding interactions with water molecules and coordinates in a geometry where one of its oxygen atoms is double bonded to two nitrogen atoms. This structural analysis suggests that 4 CB may bind to tyrosinase through adsorption mechanism.</p>

3-Chloro-2-methylaniline is an organic chemical that is used as a raw material in the production of pesticides and pharmaceuticals. 3-Chloro-2-methylaniline is generated by the reaction of hydrochloric acid with isobutyl chloride, which produces a mixture of chloroalkylcarbinols. This product can be activated to form chloromethylketones or chloromethylcarbonyls by reacting it with sodium hypochlorite or hydrogen peroxide. The impurities found in 3-Chloro-2-methylaniline are mainly carbon sources and inorganic compounds such as chloride and strain. It can be synthesized from other chemicals and also through chromatographic science.

<p>Please enquire for more information about 2-Chloro-4-fluoropyridine-5-boronic acid, pinacol ester including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Creatine phosphate di(tris) salt is a cyclase and rectifier of potassium ion channels. It is a potent activator of calcium ion channels, expressed in the cells of the ng108-15 mouse neuroblastoma line. Creatine phosphate di(tris) salt also potently activates guanylate cyclase and l-type calcium ion channels. This drug has been shown to stimulate prostaglandin synthesis and inhibit the production of prostaglandin E1 in biological chemistry studies. Creatine phosphate di(tris) salt is a cyclase and rectifier of potassium ion channels. It is a potent activator of calcium ion channels, expressed in the cells of the ng108-15 mouse neuroblastoma line. Creatine phosphate di(tris) salt also potently activates guanylate cyclase and l-type calcium ion channels. This drug has been shown to stimulate prostaglandin synthesis and inhibit the production of prostaglandin E1 in</p>

<p>1-[(4-Chlorophenyl)phenylmethyl]piperazine is an analytical reagent that is used in the determination of meclozine, a drug used for the treatment of nausea and vomiting. 1-[(4-Chlorophenyl)phenylmethyl]piperazine is a nucleophile, which means that it can donate electrons to other molecules. It can be used as a catalyst to increase the rate of chemical reactions. 1-[(4-Chlorophenyl)phenylmethyl]piperazine may also be used in wastewater treatment because it has been shown to have phospholipidosis inhibiting properties. The levorotatory form (1R-enantiomer) of this compound has been shown to inhibit protein synthesis in vitro and is an amine oxidase inhibitor that binds to proteins with nitrogen atoms. This nucleophilic compound may also be converted into an n-oxide or dinucleotide phosphate by hydrochloric acid and</p>

<p>4-Chlorophenylacetylene is a compound that is created by the reaction of chloroform and acetylene. The reaction yield can be increased by using a catalytic amount of silicon, which increases the rate of hydration. Terminal alkynes react with 4-chlorophenylacetylene to form polymers, which are insoluble in most solvents. 4-Chlorophenylacetylene has been shown to have inhibitory activity against the growth of bacteria and fungi when tested in model species such as Escherichia coli and Saccharomyces cerevisiae.</p>

<p>alpha-Cyano-3-hydroxycinnamic acid is a mitochondrial matrix analog that has been shown to inhibit the uptake of carnitine, glutamate, and branched-chain amino acids. This compound also inhibits the activity of glyceraldehyde-3-phosphate dehydrogenase and dodecyl CoA dehydrogenase, which are enzymes involved in the production of cellular energy. alpha-Cyano-3-hydroxycinnamic acid also inhibits the synthesis of mitochondrial DNA and RNA. The compound binds to the enzyme succinate dehydrogenase, inhibiting its function. This inhibition leads to a decrease in cellular energy production and an increase in oxidative stress.</p>

<p>Versatile small molecule scaffold</p>

Versatile small molecule scaffold

<p>Versatile small molecule scaffold</p>

<p>4-Methyl-N-(prop-2-yn-1-yl)benzenesulfonamide is a chiral, isopropyl substituted sulfonamide that has been synthesized by a palladium-catalyzed coupling reaction. It is an example of a biomolecular catalyst that has been shown to have the ability to catalyze the formation of chlorides, terminal alkynes and formyl groups. The crystal structure of this compound has been determined by X-ray diffraction and it was found to be composed of two molecules in the asymmetric unit with one molecule being disordered. 4-Methylbenzenesulfonamide is also an alkylating agent and can react with amines and amides to form cinchona alkaloid derivatives.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>2,4-Dibromobut-1-ene is a dihedral molecule that is used as an intermediate in the synthesis of other compounds. The highest serum levels are seen in infants and rationalized to protonation of the tertiary butyl group. Dehydration leads to formation of a high yield via alkylation with long-term exposure. 2,4-Dibromobut-1-ene has been shown to be an antineoplastic drug that inhibits cell growth by binding to electron deficient positions on DNA molecules. This causes nucleic acid strand breakage and inhibition of DNA synthesis, leading to cell death.</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>

Versatile small molecule scaffold

<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>1-Bromocyclohexanecarboxylic acid is a member of the class of organic compounds known as carboxylic acids. It is an oxygenated compound that contains the carboxyl group (-COOH). It has been used to synthesize a number of other organic compounds. 1-Bromocyclohexanecarboxylic acid also reacts with metal salt to form phosphine, which can be used as a reducing agent in organic reactions. The conformation and reactivity of 1-bromocyclohexane can be predicted using theory and calculations. Hydrocarbon groups are added by diisocyanate, which react with hydrocarbon catalytically to produce benzene. This reaction can be used for analgesic or carbamate production.</p>

<p>Versatile small molecule scaffold</p>

<p>1,1'-(2-Hydroxy-5-methyl-1,3-phenylene)diethanone is a dioxime ligand that binds to metal ions in a stereochemical fashion. This compound has been shown to bind to the Fe ion and to undergo an intramolecular hydrogen transfer reaction. 1,1'-(2-Hydroxy-5-methyl-1,3-phenylene)diethanone has also been used as a macrocycle that can be assembled into supramolecular structures with metal ions. This molecule is magnetic and its magnetic properties have been studied by electrochemical methods.</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>Methyl 3-methyl-4,5-dihydro-1,2-oxazole-5-carboxylate (MMDC) is a heterocyclic compound that is used as a raw material for the production of various chemicals. It can be used to produce aniline and acetaldehyde. MMDC is also used in the synthesis of other heterocyclic compounds, such as methyl 2-(3,4-dimethoxybenzoyl)-1H-imidazole-5-carboxylate. This chemical has been found to be an effective inhibitor of bacterial nitrite reductase activity.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>5-Methyl-5-hexenoic acid is a synthetic chemical that can be used as a marker for biochemical pathways. It is synthesized from hydrochloric acid and boron trifluoride etherate, which are heated together at 130°C until all the HCI has been evaporated. 5-Methyl-5-hexenoic acid is then reacted with an amide to produce a fatty acid. Oxazolidinones are often used to synthesize this compound, although it can also be made through dehydrating and anhydrous sodium chloride. The product contains impurities and diastereomers that must be removed before it can be used in the manufacture of pharmaceuticals.</p>

2-Bromo-3,4-dimethoxybenzaldehyde (BDMB) is a fluorescent aldehyde that can be used as an analog for 2,4-dinitrofluorobenzene. It has been shown to have cytotoxic effects on cancer cells. BDMB binds to microtubules and inhibits their polymerization and depolymerization, preventing the formation of the cytoskeleton in the cell. This leads to cell death by apoptosis. The affinity of BDMB for microtubules is much higher than its affinity for other cellular components. BDMB also has been shown to inhibit DNA synthesis in cancer cells through inhibition of RNA polymerase II transcription.

<p>Versatile small molecule scaffold</p>

<p>Phenyl-6H-1,3,4-thiadiazin-2-amine is a bidentate ligand that has been used in analyses to study the binding of various substances. It is a phenolic compound with an azomethine group and nitrogen atoms. Phenyl-6H-1,3,4-thiadiazin-2-amine can be synthesized by reacting 1,5-diaminonaphthalene with 2,6-dihydroxyphenol. This reaction can be followed by elemental analysis and elemental identification. Phenyl-6H-1,3,4-thiadiazin-2 amine also has magnetic properties and phenolic oxygen. It displays thermogravimetric properties that can be analyzed using a TGA instrument. The electronic spectra of this substance can also be analyzed using UV/Vis spectroscopy or NMR spectroscopy. Phenyl-[H]-</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

Versatile small molecule scaffold

<p>2-(4-Formylphenyl)acetonitrile is a nucleophilic solvent that can react with benzyl alcohol in the liquid phase. It is used to produce benzaldehyde and toluene by hydrogenating benzyl alcohol. 2-(4-Formylphenyl)acetonitrile has a constant boiling point, which makes it useful for adsorption. It also reacts with hydrogen in the presence of a catalyst to produce benzylamine and hydrogen gas. The kinetic study of this reaction has shown that it follows first order kinetics.</p>

<p>Versatile small molecule scaffold</p>

<p>2-(2-Hydroxy-ethoxy)-benzoic acid is a semicrystalline solid with a melting point at about 220°C. It has a concentration range of 0.5 to 10% and a molecular weight of 192.2 g/mol. 2-(2-Hydroxy-ethoxy)-benzoic acid has been used as an additive in polymers and copolymers, lowering the transition temperature of the polymer or copolymer. The compound has also been used as an intermediate in the synthesis of other compounds such as amorphous polymers, polycaprolactone, and polyesters. 2-(2-Hydroxy-ethoxy)-benzoic acid is an organic compound that belongs to the group of benzoic acids and can be synthesized by reacting ethylene glycol with phthalic anhydride.</p>

<p>Ethyl 2-hydroxy-3-methylbenzoate is an organic compound with the chemical formula CH3COCH2CH(OH)COOH. It is a colorless liquid that is soluble in alcohol, ether, and chloroform. It has been used as a precursor to salicylic acid and other compounds with similar function. This product can be synthesized by cyclization of enol ethers with acid derivatives or by cyclization of alkyl phenols with anhydrides. Cyclization reactions are efficient, requiring only a few steps and high temperatures. Salicylic acid can also be obtained from ethyl 2-hydroxy-3-methylbenzoate via hydrolysis of the ester group, which then undergoes decarboxylation to form salicylic acid.</p>

<p>4-Phenylpyridine-2-carboxaldehyde (4PA) is a crystalline compound with a molecular weight of 198.3. It has been shown to have intramolecular hydrogen bonds and intermolecular hydrogen bonds, which are responsible for the formation of the crystal structure. 4PA is most commonly found in acetone, thiourea, and other organic solvents. The diffraction data for this molecule were obtained using x-ray diffraction methods.</p>