Building Blocks

<p>Please enquire for more information about 4-Bromo-3-(trifluoromethoxy)pyridine hydrobromide including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>1-Bromo-4-iodobenzene is an aryl halide that can be synthesized by the cross coupling of ethyl formate and hydrochloric acid. This compound is useful in analytical applications, such as chromatographic methods, due to its high solubility in organic solvents. It is also used in synthetic procedures for the preparation of other aryl halides. 1-Bromo-4-iodobenzene has been used to synthesize calcium carbonate via the Suzuki coupling reaction with sodium salts, which are nucleophiles. The carbonyl group on this molecule reacts with the nucleophile, forming an alkyl group and a metal salt. Transfer reactions involving these salts can produce other products with different functional groups.</p>

<p>2-Bromo-5-hydroxypyridine is an aromatic compound that is used in the synthesis of a variety of pharmaceuticals and other organic compounds. It can be synthesized by the Suzuki coupling reaction from 2-bromobenzaldehyde and 5-aminopyridine. 2-Bromo-5-hydroxypyridine has been shown to be a hepatotoxin in humans, with possible carcinogenic activity. It also has cholinergic properties, as well as being able to cause fluorescence when exposed to halogens. The carbon next to the hydroxyl group is a stereocenter, so there are two different configurations for this molecule. The configuration shown above (R) is the more stable form of this molecule due to its electron withdrawing power on the neighboring oxygen atom.</p>

<p>(1R)-2-Chloro-1-(2,4-dichlorophenyl)ethan-1-ol is a substrate for acetylation that is used in the synthesis of enantiopure alcohols. It has been shown to be an inhibitor of alcohol dehydrogenases and hydrophobic alcohols. (1R)-2-Chloro-1-(2,4-dichlorophenyl)ethan-1-ol has also been found to be active against fungi such as Penicillium chrysogenum and Cryptococcus neoformans. This compound is stereoselective when used as an antifungal agent, which means it will only inhibit one enantiomer of a molecule.</p>

<p>N-(4-Aminophenyl)-N-methyl-2-(4-methylpiperazin-1-yl)acetamide is an environmental and industrial chemical that is used as a formate, benzoate, and methyl benzoate intermediate. It reacts with nitric acid to form N-(4-aminophenyl)-N-methyl-2-(4-nitrophenoxy)acetamide (NPA). NPA has been shown to have antiangiogenic properties. NPA inhibits the proliferation of endothelial cells by interfering with the cell cycle and inducing apoptosis.</p>

<p>Please enquire for more information about 2-Bromobenzo[d]thiazol-6-amine including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Leu-Leu-Leu-OH is a pentapeptide that is used in cancer treatment to inhibit the growth of cancer cells. It prevents the production of proteins and, as a result, cell division. Leu-Leu-Leu-OH has been shown to be effective against tumor cells with an antibody that binds to the surface of cells. The monoclonal antibody is taken up by the cancer cells through receptor mediated endocytosis, which leads to inhibition of protein synthesis and cell death.</p>

<p>Fmoc-a-Me-Lys(Boc)-OH is a versatile building block that can be used in the synthesis of complex compounds. It is a reagent and speciality chemical, which are substances used in research laboratories. Fmoc-a-Me-Lys(Boc)-OH has been used as an intermediate in the synthesis of drugs such as antihypertensive agents, anticonvulsants, and antibiotics. It has also been used as a reaction component in organic syntheses to produce peptides, polymers, and other compounds with biologically active properties.</p>

<p>Versatile small molecule scaffold</p>

<p>Timonacic is an analog of nicotinamide that has been shown to be an effective inhibitor of energy metabolism in the mitochondria. It has antioxidative properties and can protect against the development of heart disease by inhibiting the production of reactive oxygen species. Timonacic's anti-inflammatory properties may be due to its ability to inhibit prostaglandin synthesis. It also has a high affinity for fatty acids, which may contribute to its inhibitory effects on lipid peroxidation. This drug has a carboxy terminal and is used as a sodium salt, which may play a role in its enzyme inhibition activity. Timonacic inhibits the activities of enzymes such as carnitine acetyltransferase and pyruvate dehydrogenase kinase, which are involved in the biosynthesis of fatty acids. The intramolecular hydrogen bonds formed with timonacic may contribute to its inhibitory effect on these enzymes.</p>

<p>Diethyl Acetylphosphonate is a synthetic chemical that is used in the production of ethyl esters, which are used as intermediates for the production of epoxides. It has shown to be a bidentate ligand and reacts with primary amines. Diethyl Acetylphosphonate can be made by reacting phosphorus pentachloride with ethyl acetate and hydrochloric acid. The reaction mechanism is similar to that of other organophosphorus compounds, in which a phosphine oxide intermediate reacts with an organic halide. Diethyl Acetylphosphonate has shown to be effective in detergent compositions and triethyl orthoformate, as well as alkanoic acid.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>N-butyl methanesulfonate is a genotoxic agent that inhibits the growth of bacteria by binding to the DNA. N-butyl methanesulfonate is effective against typhimurium and has shown carcinogenic effects in hamster cells. N-butyl methanesulfonate is also capable of inhibiting quinoline derivatives, which are carcinogens that are found in tobacco smoke. This chemical can be used as a natural compound for the treatment of diabetic neuropathy and cryptococcus neoformans. It may also be used as an antiviral agent for the treatment of influenza virus.</p>

<p>(2S,6S)-2,6-Dimethylmorpholine is an optically pure compound that can be used to optimize the epoxidase reaction. It belongs to the class of morpholines and has two enantiomers. The (2R,6R)-enantiomer is more active than the (2S,6S)-enantiomer in catalyzing the epoxidase reaction. The temperature optima for both enantiomers are different with the (2R,6R)-enantiomer having a higher optimal temperature than the (2S,6S) enantiomer. This compound can be used as a chiral auxiliary to separate racemic mixtures by focusing on one enantiomer at a time. It can also be used as an analytical method for determining plate number and plate height.</p>

<p>Versatile small molecule scaffold</p>

<p>4-Hydroxy-5-methoxy-2-nitrobenzaldehyde (4HMN) is a proton donor that can be used as a crosslinking agent. It is an acidic compound that binds to the substrate, usually via hydrogen bonds. 4HMN has been shown to have good binding affinity for tumour cell lines and can be used as a crosslinking agent in bioconjugation reactions. It is also a reversible chemical reaction, which means it can be hydrolyzed under certain conditions. 4HMN has been shown to be capable of enhancing the rate of enzymatic reactions by acting as a cofactor or coenzyme, such as degradable enzymes and enzymes with low turnover rates. The kinetic process of these reactions are measured by fluorescence techniques and gel permeation chromatography.</p>

<p>FG-2216 is a peptide that activates the G protein-coupled receptor, leading to increased intracellular calcium. FG-2216 is a potent agonist of the GPRC6A receptor and has been shown to inhibit pain perception in animal models. FG-2216 has been shown to have no effect on ion channels and does not affect cellular proliferation or migration. FG-2216 may be useful as a research tool for studying the function of the GPRC6A receptor in animal models.</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>Bromo-PEG3-azide is a PEG compound with two different functional groups (also known as heterobifunctional). Unlike homobifunctional PEG compounds (same functional group on both ends), this type of compounds are more versatile as have two different anchor points. Bromo-PEG3-azide is used as a linker and spacer to add a PEG moiety, via pegylation (a bioconjugation technique) to proteins, peptides, oligonucleotides, small molecules and nanoparticles.</p>

<p>2-Bromo-3-hydroxy-benzaldehyde is a nitrate that has been shown to have anti-cancer properties. It inhibits the growth of cancer cells by binding to bromodomains in their DNA, thereby preventing transcription and replication. 2-Bromo-3-hydroxy-benzaldehyde also inhibits the production of nitric oxide, which may lead to an inhibitory effect on tumour angiogenesis. The stereoisomers of this compound are used as precursors for the synthesis of ammonium nitrate, which is used as a fertilizer and explosive. 2-Bromo-3-hydroxy-benzaldehyde is also used in organic synthesis as a precursor for acetylation or halide reactions with palladium complexes or halides.</p>

<p>Versatile small molecule scaffold</p>

<p>2-Oxohexanoic acid (2-OHBA) is a fatty acid that is synthesized from the amino acids lysine and methionine. It is involved in mitochondrial metabolism and has been found to be necessary for spermatozoa motility. 2-OHBA has been shown to inhibit the activity of glutamate dehydrogenase, an enzyme that catalyzes the conversion of glutamate to α-ketoglutarate, which is required for energy production. This inhibition leads to a decrease in ATP levels, which may cause a variety of symptoms, including fatigue and weight loss. Furthermore, 2-OHBA inhibits protein synthesis by blocking the incorporation of amino acids into proteins. The inhibition of this process can lead to high ammonia levels in the blood and accumulation of other nitrogenous wastes in tissues such as liver or muscle tissue. Analysis of urine samples has shown that 2-OHBA is excreted unchanged in urine.</p>

<p>2,2-Dipropylpentanoic acid is a white crystalline solid with a melting point of -51°C. It has a hydroxyl group and an ester linkage. The chemical formula is CH3(CH2)3COOC3H7. It has a molecular weight of 182.27 g/mol and a density of 1.071 g/cm3. It is soluble in organic solvents such as chloroform, ether, benzene, acetone, and carbon tetrachloride but insoluble in water. 2,2-Dipropylpentanoic acid can be used as a catalyst for the synthesis of polymers from monocarboxylic acids and chloride or magnesium halides. This compound also has antidepressant activity by inhibiting the reuptake of serotonin from the synapse into the presynaptic neuron.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>2-Methylthiazole-4-carboxaldehyde is an aldehyde that is the product of the condensation of 2,4-dibenzoylacetone and acetone in the presence of diazomethane. It has been used as a precursor to other compounds such as benzoyl chloride, glyoxal, and aldehydes. 2-Methylthiazole-4-carboxaldehyde can be synthesized using acetylation or nitration of thiols or with glyoxal or aldehyde. The reactivity of this compound is high and can be carried out in high yield.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>1,4-Cubanedicarboxylic acid is an organic compound that is a diacid. It has been shown to be an inhibitor of chloride secretion in the intestine, and can also decrease the rate at which hydrogen ions are released into the intestinal lumen. 1,4-Cubanedicarboxylic acid is also a cross-linking agent that can be used in organic solvents for large-scale synthesis. The optical properties of 1,4-cubanedicarboxylic acid have been studied using FTIR spectroscopy. This agent has been found to react with intramolecular hydrogen to form a six membered ring.</p>

<p>2-Chloro-2-(chlorodifluoromethoxy)-1,1,1-trifluoroethane (HFC-152a) is a chemical compound that belongs to the group of chlorofluorocarbons. It has been used as a refrigerant and aerosol propellant. HFC-152a is an azeotrope with methyl ethyl ketone and ethyl ketone. It has also been reported to have properties as an ether, acetone, and difluoromethyl.</p>

<p>(S)-2-Bromobutyric acid is a chiral compound. It is an enantiomer of the biologically inactive (R)-2-bromobutyric acid. The (S)-enantiomer has been shown to exhibit biological activity, with a kinetic and detectable activity that are similar to those of the parent molecule. This compound can be used as a precursor for pharmaceuticals, such as antibiotics, which would be useful in cases where bacteria have developed resistance to existing antibiotics. The dehalogenase enzyme catalyzes the hydrolysis of halogenated aromatic compounds in a way that produces an alcohol and hydrogen bromide. This reaction can be detected by changes in the chemical properties of the environment or by detecting changes in the optical rotation or fluorescence of the product.</p>

<p>Methyl 4-fluorothiophene-2-carboxylate is a fluorinated organic compound that is used as a model compound in polymer chemistry. It has been used to synthesize polymers with stepwise fluorination and diketopyrrolopyrrole moieties. This molecule also has optoelectronic properties and can be converted to a conjugated, monofluorinated, or difluorinated form by the addition of electron-withdrawing groups such as nitro or cyano groups. Methyl 4-fluorothiophene-2-carboxylate is an acceptor for electron transfer reactions.</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>(S)-(-)-1-Phenylpropylamine is a compound that can be synthesized by the asymmetric synthesis of 1-phenylethylamine. It is an amine that is used in the production of other compounds and has been shown to be reactive with a number of different compounds. The chemical profile of (S)-(-)-1-Phenylpropylamine consists mainly of aldehydes, amides, amines, and alkylating agents. This chiral molecule can be used for the production of drugs or as a precursor for other chemicals.</p>

<p>5-bromo-3,3-dimethyl-2,3-dihydro-1H-indole is an activator that is used in palladium catalyzed reactions to form a phosphine ligand. 5-bromo-3,3-dimethyl-2,3-dihydro-1H-indole is also used as a vasotropic agent and reagent for organic synthesis. It is used to synthesize ethylesters and salts of 5-(5'-bromo)-2,2'-dihydroquinoline carboxylic acid. This compound can be hydrolyzed with alkaline solution to produce the corresponding amine.</p>

<p>Ethyl cyclopropaneacetate is an organic compound that belongs to the class of aminophenyl ethyl esters. It has been shown to inhibit neutrophil migration and angiotensin II-induced vasoconstriction in cerebral arteries, suggesting that it may have a role in the treatment of chronic bronchitis. Ethyl cyclopropaneacetate has also been shown to have antimycotic activity against Candida albicans and Aspergillus niger, as well as cancer-fighting effects. This compound is synthesized by reacting triethyl orthoformate with adenosine under mild conditions. The reaction system is high yielding and can be used for the synthesis of other drugs.</p>

<p>Versatile small molecule scaffold</p>