Building Blocks

<p>Veterinary drug, ectoparasiticide</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>2-Chloro-3-(hydroxymethyl)pyridine is an organic compound that is used as a building block for the synthesis of other heterocycles. This compound can be synthesized from 2-chloronicotinic acid, which is obtained by oxidation of nicotine with sodium hypochlorite in the presence of potassium ion. The reaction proceeds via a cleavage of the C-Cl bond and formation of a pyridine ring. The catalytic process can be performed at room temperature and at atmospheric pressure in a variety of solvents, including water.<br>2-Chloro-3-(hydroxymethyl)pyridine has been shown to have high yields for the preparation of compounds such as 2,4-dichloropyridine and 4,5-dichloropyrimidine. It also has been used in the preparation of pharmaceuticals such as atrial natriuretic factor (ANF).</p>

<p>Please enquire for more information about 6-Chloro-pyridazine hydrochloride 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>Di(1-adamantyl)chlorophosphine is a bifunctional ligand that can be used for the palladium-catalyzed coupling of aryl chlorides and amines. Di(1-adamantyl)chlorophosphine is synthesized from adamantane, phosphorous pentachloride, and anhydrous ammonia in the presence of catalytic amounts of palladium. Di(1-adamantyl)chlorophosphine is immobilized on silica gel to prevent hydrolysis. This ligand reacts with primary amines to form iminophosphoranes, which can then be reacted with aryl chlorides to form aryl chloroamines.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>1-Cyano-4-(dimethylamino)benzene is a molecule that has been shown to inhibit the growth of hamster v79 cells. It also inhibits the synthesis of DNA and RNA. The binding constants for this molecule have been determined to be 1.0 x 10^9 M^-1, with an n-octanol/water partition coefficient (log P) of 5.5. This molecule is soluble in nonpolar solvents and may be used as a model system for hydrogen bonding interactions or reaction mechanisms in organic chemistry. This compound contains a deuterium isotope and can be used to study the effects of hydrogen bonding on reactions in organic chemistry at high temperatures, with the use of preparative hplc.</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>3,4-Diaminobenzophenone is an unsymmetrical compound and a derivative of benzophenone. It is used in the synthesis of other organic compounds, such as pharmaceuticals. 3,4-Diaminobenzophenone is also used as a solubilizing agent for drugs that are insoluble in water. The molecular weight of 3,4-Diaminobenzophenone can be determined by gravimetric analysis or FTIR methods. 3,4-Diaminobenzophenone has been shown to have antioxidative properties. This molecule can bind to hydroxyl groups on biomolecules and protect them from oxidation by reactive oxygen species (ROS).</p>

<p>1,3,5,7-Tetrabromoadamantane is a molecule that has been synthesized and introduced as a mediator to introduce oxidants. The introduction of the oxidant is mediated by 1,3,5,7-tetrabromoadamantane. This molecule has been shown to be synthesized in two steps from hexamethylenetetramine (HMT) and iodomethane. The synthesis of this molecule can also be achieved by reacting synthons such as tetraphenylmethane with hydrochloric acid. 1,3,5,7-Tetrabromoadamantane is an equivalence mediator because it can mediate a redox reaction in which the oxidizing agent is reduced and the reducing agent is oxidized.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>3,5-Dihydroxy-4-methylbenzoic acid is an efficient synthesis of the natural product lucidin. It is a quinone that is found in citrifolia and morindone, compounds which are used as analgesics and antipyretics. This compound has been shown to inhibit the growth of fungi by inhibition of protein synthesis. 3,5-Dihydroxy-4-methylbenzoic acid also inhibits the production of citric acid cycle intermediates such as succinic acid and fumaric acid.</p>

<p>3,5-Dihydroxybenzaldehyde (DHBA) is a plant metabolite that is classified as a phenolic compound. It is found in many plants and has important biological functions such as the production of carotenoids or the cleavage of carotenoid to form other compounds. DHBA can be extracted from plant tissue with hydrochloric acid or carbon sources. It has been shown that DHBA inhibits the growth of soil bacteria by binding to amines and thus preventing them from reacting with substrates. This may be due to its ability to act as an electron donor, which could also explain its inhibitory activity on carotenoid cleavage.</p>

<p>Disodium 8-amino-1,3,6-naphthalenetrisulfonate is a fluorescent sensor that can detect albumin in human serum. Disodium 8-amino-1,3,6-naphthalenetrisulfonate selectively detects the molecule albumin in blood with a sensitivity of approximately 1.5 nmol/L and a selectivity of nearly 100%. The fluorescent sensor consists of an immobilized nanometer sized molecule of 8-aminonaphthalene trisulfonic acid on hydrotalcite. The sensor has been shown to be selective for albumin and does not react with other serum proteins such as immunoglobulins or fibrinogen.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>2-Ethynyl-3-methoxypyridine is a chiral, alkynyl compound that can be synthesized from the reaction of acetone and ethyne. This compound is axially chiral and has two rotational isomers, which are optically active. The synthesis of this compound was first reported in 1952 by cyclizing 2-ethynylpyridine with methoxyacetophenone in the presence of acetic acid. The photochemical reactions of this compound have been studied extensively and it has shown to be a useful substrate for pyridines.</p>

<p>2,6-Dimethoxyisonicotinic acid is a cytotoxic agent that is structurally related to colchicine and combretastatin A-4. It has been shown to induce apoptosis in cancer cells by inhibiting the polymerization of tubulin. This drug also inhibits the proliferation of cancer cells by binding to DNA and disrupting the synthesis of proteins necessary for cell division. The inhibitory effect on protein synthesis may be due to its ability to inhibit the activity of RNA polymerase II and III, which are essential for transcription. 2,6-Dimethoxyisonicotinic acid also induces an anticancer effect through its ability to bind to phenolic moieties and inhibit the growth of cancer cells.</p>

<p>2,4,5-Trimethoxybenzylamine is a synthetic compound that can be used as a precursor to the synthesis of other chemicals. It is prepared by reacting phenol with deuterium gas in a process called amination. This reaction is followed by reductive quaternization with cyanide. 2,4,5-Trimethoxybenzylamine is often used as an intermediate for the synthesis of drugs such as tamoxifen and clonidine.</p>

<p>2,2',4,4'-tetrahydroxybenzophenone is a hydroxylated benzophenone that has immunomodulatory effects. It binds to the receptor in the immune system and can cause an increase in cytokine production. 2,2',4,4'-tetrahydroxybenzophenone is cytotoxic and has significant toxicity in vitro. The molecule has been shown to disrupt mitochondrial membrane potential. This may be due to its ability to form hydrogen bonds with molecules on the mitochondrial membrane. 2,2',4,4'-tetrahydroxybenzophenone also modulates transcriptional regulation of genes involved in cell proliferation and apoptosis. The drug is detectable at low levels by mass spectrometry and is not known to have any toxicological effects.END&gt;&gt;</p>

<p>2,4,6-Trichloropyrimidine is an antimicrobial agent that belongs to the chemical class of pyrimidine compounds. It inhibits bacterial growth by cross-linking with amino acids and nucleic acids in the cell wall, thereby inhibiting protein synthesis. 2,4,6-Trichloropyrimidine is also a cross-linking agent for polymers such as polyurethane and vinyl chloride. This compound has been shown to be effective against P. aeruginosa and other bacteria that are resistant to antibiotics. 2,4,6-Trichloropyrimidine reacts with water vapor or oxygen nucleophiles to form hydrogen chloride and amine groups. These reactions can be used for identification of this compound in the laboratory.</p>

<p>Please enquire for more information about Tert-butyl N-(8-bromooctyl)carbamate including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>1,2,3,4-Tetrahydropyridin-4-one is an organic compound that can be synthesized by a cross-coupling reaction between a pyridine and chloroformate. The reaction mechanism involves nucleophilic addition of the amine to the electrophile followed by reductive elimination. This process leads to the formation of a tetrahydroquinoline skeleton with stereoselectivity. Tetrahydropyridin-4-one can also be synthesized from an iminium ion or an activated pyridinium salt. The resulting product will have a different skeleton because it was synthesized through different mechanisms.</p>

<p>Sodium 4-hydroxybenzenesulfonate dihydrate is a hydrogenated compound with reactive properties. It is used in the production of optical materials and is used to produce hydrogen peroxide, which is a strong oxidizing agent. Sodium 4-hydroxybenzenesulfonate dihydrate has been shown to react with calcium ions to form calcium sulfinates. The luminescence property of this compound can be enhanced by mixing it with other compounds such as x-ray diffraction study, functional groups, or hydrogen peroxide. The reaction time for the formation of sodium 4-hydroxybenzenesulfonate dihydrate can be shortened by adding anions such as sulfamic acid.</p>

<p>2,4-Dinitrophenylacetic acid is a chemical substance with the potential to inhibit acetylation. It can be used as an antigen and has been detected in environmental chemistry. 2,4-Dinitrophenylacetic acid is produced by the reaction of chemicals that are found in the environment and it can be detected at low concentrations. This compound is able to react with proteins in cells, leading to high cytotoxicity. 2,4-Dinitrophenylacetic acid can also stabilize optical systems.</p>

<p>2,4-Dichloro-3-nitropyridine is a halogenated pyridinium salt that has been shown to inhibit the influenza virus in vitro. This compound is also reactive with nucleophilic groups such as amines, alcohols, and thiols. 2,4-Dichloro-3-nitropyridine has been used for the synthesis of quinoline derivatives that have potential applications in autoimmune diseases or cancer. 2,4-Dichloro-3-nitropyridine has also been found to be an inhibitor of tumor necrosis factor alpha (TNFα) production by LPS stimulated human monocytes.</p>

<p>Fipexide is a dopamine analog that is used as an anti-inflammatory drug. Fipexide has been shown to be effective against inflammatory bowel disease, autoimmune diseases and chronic oral toxicity in animal models. The symptoms of fipexide are similar to the symptoms of Parkinson's disease, which include tremors, muscle rigidity and slowness of movement. Fipexide also has a reactive nitrogen atom in its molecular structure, which may contribute to its toxicity. It has been shown to have no effect on locomotor activity in animals with bowel disease.</p>

<p>Versatile small molecule scaffold</p>

<p>4,5-Dihydroxy-2,3-pentanedione is a carbonyl compound that is the product of the oxidation of ascorbic acid. It is used in wastewater treatment and has antimicrobial properties against infectious diseases. This compound has been shown to inhibit protein synthesis by binding to the ribosome and preventing the formation of peptide bonds between amino acids. 4,5-Dihydroxy-2,3-pentanedione has also been shown to bind to plasma proteins, which may be due to its acyl chain structure. 4,5-Dihydroxy-2,3-pentanedione can be synthesized in a catalytic mechanism that involves dehydroascorbic acid and molecular oxygen.</p>

<p>Versatile small molecule scaffold</p>

<p>Ecamsule is a broad spectrum sunscreen agent that is used to protect skin from the harmful effects of ultraviolet radiation. It is a synthetic chemical compound with a molecular structure consisting of an octocrylene core and an organic side chain. Ecamsule is applied to the skin in the form of microcapsules and protects against UVA and UVB rays by absorbing them or by reflecting them away. The efficacy of this product has been shown in clinical studies on humans. Ecamsule has shown no adverse reactions in humans, but toxicological studies have not been conducted.</p>

<p>Versatile small molecule scaffold</p>

<p>1,2,3,4,5-Pentaphenyl-1'-(di-tert-butylphosphino)ferrocene (Pd(dba)2) is a reagent in the form of a dark brown liquid that can be used to synthesize benzene derivatives. It has been shown to be soluble in chloroform and toluene. This compound is stable at room temperature and it can be eluted with phenyl chloride. Pd(dba)2 is a ligand that binds to the metal palladium in order to facilitate the formation of complex compounds.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Decahydroquinoxaline is a heterocyclic compound that contains a nitrogen atom in its structure. The hydroxyl group on the ring can act as an electron-donating group, which can be important for receptor binding and neurotransmission. It also has anti-inflammatory properties. Decahydroquinoxaline has been shown to have anticancer and anti-inflammatory effects, as well as being used for the treatment of chronic arthritis, bowel disease, and dopamine production.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Please enquire for more information about H-Ser-Ala-Glu-Glu-Tyr-Glu-Tyr-Pro-Ser OH trifluoroacetate 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>