Building Blocks

<p>Cyclobutanesulfonyl chloride is a reagent that is used for the synthesis of 1-6-alkylcyclobutanes. It can be used to synthesize heterocyclic compounds, including those with high optical purity. Cyclobutanesulfonyl chloride has been shown to have antiviral and antiproliferative properties. It has also been shown to exhibit anticancer activity in vitro and in vivo. The mechanism of action for this compound is unclear, but it may inhibit protein synthesis by attacking the amino acid methionine in proteins or by inhibiting DNA replication.</p>

<p>Please enquire for more information about 2-Bromo-1-(4-chloro-3-fluorophenyl)ethanone 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>Cyclopent-2-en-1-ol is a reactive monomer that can react with chloride and hydroxyl groups. It can also undergo reaction with sodium carbonate to form a cyclic ester. Cyclopent-2-en-1-ol can be converted to an epoxide by the use of acid catalyst. This compound also has the ability to polymerize, forming polymers that are used in rayon production.</p>

<p>Cucurbit[7]uril is a chemical compound that can be used as a fluorescent probe for protein target. It has been shown to produce significant cytotoxicity against cancer cell lines in vitro. Cucurbit[7]uril also exhibits hydrophobic effects, which bind to the cell nuclei of cancer cells and inhibits DNA replication. The photophysical properties of cucurbit[7]uril are stable under physiological conditions and it can be used in vivo as a styryl dye. This chemical compound is also able to form stable complexes with carbonyl oxygens, making it an interesting candidate for anti-cancer drug development.</p>

<p>4-Chloro-3-nitroquinoline is a quinoline derivative that can be synthesized by cross-coupling reaction. The amide and n-oxide functional groups are the most reactive sites. It can react with nucleophiles such as haloamines, azides, and pyridazines to form covalent bonds. 4-Chloro-3-nitroquinoline has been shown to have anti-HIV activity in vitro and in vivo in animal models. In addition, this compound has shown potential use for the treatment of leishmania.</p>

<p>4-Chloro-8-quinolinol is a quinoline derivative that has been shown to have pharmacological effects. It is used in the synthesis of other compounds, such as 5-chloro-8-hydroxyquinoline, which is used in the treatment of cancer. 4-Chloro-8-quinolinol can also be prepared by oxidizing 5,6,7,8 tetrachloroquinoline with chlorine and ammonia. The photophysical properties of this compound are analogous to those of benzothiazole derivatives. The fluorescence emission spectrum ranges from 360 nm to 450 nm with a maximum at 390 nm and emission intensity at 350 nm. This compound exhibits fungitoxicity against Penicillium notatum and Aspergillus fumigatus.</p>

<p>2-(Chloromethyl)-4-methoxy-3,5-dimethylpyridine hydrochloride is a benzimidazole derivative. It has a chemical stability and can be used for wastewater treatment. It is also a pump inhibitor and can be used for anhydrous sodium magnesium salts. This product is synthesized from the reaction of protonated 2-bromo-4-methoxyphenol with 2,6-dimethylpyridine in the presence of hydrochloric acid. The reaction was carried out in an asymmetric synthesis using a proton transport system. 2-(Chloromethyl)-4-methoxy-3,5-dimethylpyridine hydrochloride is soluble in water and has a pH of 1 to 3. It has been shown that this product can be used as an antioxidant and as a metal chelation agent.</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>Veterinary drug, ectoparasiticide</p>

<p>Versatile small molecule scaffold</p>

<p>2,5-Dibromopyridine is a chemical compound that can be used as a coupling agent in palladium-catalyzed cross-coupling reactions. It is used on the surface of metal particles to increase the efficiency of the reaction, and has been shown to react with substrates such as sodium hydroxide solution, sodium carbonate, halides and hydroxides. 2,5-Dibromopyridine also reacts with benzoate to form a palladium complex. 2,5-Dibromopyridine can be used as an oxidant or reductant depending on the type of reaction it is being used in. It has redox potentials at -0.6 volts for oxidation and +0.6 volts for reduction.</p>

<p>2,4-Dimethyl-3-hydroxypyridine is a hydroxypyridine compound with epoxide. It inhibits cytochrome P450 enzymes and is used as an organic solvent. 2,4-Dimethyl-3-hydroxypyridine is also used in research to study the structure of the pyridine ring and the hydroxyl group.</p>

<p>2,4-Dibromopyridine is a brominated derivative of pyridine. It is synthesized through the substitution of two bromine atoms for two hydrogens on the pyridine ring. This synthesis can be achieved by disubstitution or cross-coupling reactions. The reaction products are nucleophilic and react with electrophiles to produce substitution products. The reaction mechanism is thought to involve a six-membered transition state, which has been observed using X-ray absorption spectroscopy.</p>

<p>4,4'-Dimethyl-2,2'-bipyridine is a molecule that belongs to the group of p2 metal complexes. It has been shown to have synergistic effects with ruthenium complexes in analytical chemistry and electrochemical studies. Theoretical calculations have been performed for 4,4'-dimethyl-2,2'-bipyridine and its derivatives. These calculations show that the molecule is planar and that it can be considered as a diazonium salt. The photochemical properties of 4,4'-dimethyl-2,2'-bipyridine have also been studied in detail. This substance emits light when excited by ultraviolet light or visible light, which makes it an excellent candidate for use as a luminescent material in optical displays.</p>

<p>Diiodomethane is a chemical compound with the molecular formula CHI. It is a colorless gas that can be obtained by reacting methyl ethyl and hydroxyl group in the presence of an oxidant such as boron nitride. Diiodomethane has been used as a substrate film for n-dimethyl formamide and reaction solution, which have been studied using spectroscopic data. The product of this reaction is water vapor that leaves the system due to its low boiling point. Reaction mechanism for this process is thought to be due to the kinetic energy of the particles that collide and produce diiodomethane molecules.</p>

<p>Versatile small molecule scaffold</p>

<p>N-Carbamoyl linagliptin is a synthetic drug that is a selective, reversible inhibitor of dipeptidyl peptidase-4 (DPP-4), an enzyme that breaks down the incretin hormones GLP-1 and GIP. This drug has been shown to help control blood glucose levels in patients with type 2 diabetes. It binds to the active site of DPP-4 and prevents it from breaking down GLP-1 and GIP, which leads to increased levels of these hormones in the body. N-Carbamoyl linagliptin has a long half life, making it suitable for once daily administration. It also lacks any significant interactions with other drugs or foods.</p>

<p>Please enquire for more information about Ethyl 2-(3-phthalimidopropyl)acetoacetate 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 Edoxaban impurity G benzenesulfonate 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 Edoxaban impurity 2 p-toluenesulfonic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Ethyl 4-bromoacetoacetate is a chemical compound that is used in the synthesis of quinoline derivatives. It also has antiinflammatory properties and can be used to treat inflammatory diseases such as arthritis. The thermal expansion of this compound is greater than that of water, which can be useful in treating respiratory problems by providing increased oxygen transport. Ethyl 4-bromoacetoacetate is a reactive chemical that reacts with hydrochloric acid to produce hydrogen gas and ethyl bromide gas. It also undergoes nucleophilic substitutions at the carbon atom adjacent to the acetoacetate group. This reaction solution can be analyzed using magnetic resonance spectroscopy, which produces data on the sequences of this compound's atoms and its antiinflammatory activity.</p>

<p>Versatile small molecule scaffold</p>

<p>Please enquire for more information about Fmoc-Tyr(Et)-OH 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>C3-Ethylbenzoic acid is an organic compound that can be synthesized from the reactants ethyl bromide, propylene oxide, and acetic anhydride. The synthesis of C3-Ethylbenzoic acid is a stepwise process in which the starting materials are converted to intermediates and then reacted to form the desired product. The reaction mechanism involves bond cleavage, which generates a carboxylic acid group on one end of the molecule and a phenyl group on the other end. C3-Ethylbenzoic acid interacts with clausamine and isoprene during transport through cell membranes. This interaction may lead to increased permeability of cell membranes by c3-ethylbenzoic acid.</p>

<p>2-Ethyl-2-oxazoline is a structural analysis of 2-ethyl-2-oxazoline. It is a biocompatible polymer that has been shown to be cytotoxic to cells in culture. The mechanism for this cytotoxicity is not clear, but it may be due to the significant hydroxyl group present in the molecule. 2-Ethyl-2-oxazoline is also a pharmacological agent and can be used as an adjuvant in vaccines. This polymer has shown no significant antibody response and has water vapor permeability properties.</p>

<p>Versatile small molecule scaffold</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>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>Versatile small molecule scaffold</p>

<p>Methyl 5-hexynoate is a synthetic product that can be synthesized from soybean lipoxygenase and hydrogenation reduction. This product has been shown to be a useful synthon for the synthesis of monoclonal antibodies with high binding affinity. The synthetic pathway, which involves cross-coupling and asymmetric synthesis, is outlined in the diagram below. The following are the steps involved in the production of methyl 5-hexynoate: 1) Addition of ethyl bromide to terminal alkynes 2) Addition of hydrochloric acid 3) Reaction with potassium tert-butoxide 4) Hydrogenation reduction 5) Cross-coupling reaction 6) Asymmetric synthesis</p>

<p>8-Chlorotetrazolo[1,5-A]pyrazine is a chlorine-containing compound. It is a heterocyclic aromatic organic compound and an important intermediate in the synthesis of other compounds. 8-Chlorotetrazolo[1,5-A]pyrazine is not found in nature. The elimination of chlorine from 8-chlorotetrazolo[1,5-A]pyrazine produces benzotriazole and the molecule tetrazole. 8-Chlorotetrazolo[1,5-A]pyrazine is used as a raw material for many organic syntheses.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>5-bromo-6-methoxy-1H-indole is a synthetic, nonsteroidal compound that is structurally related to prednisolone. It has been shown to induce the synthesis of collagen by stimulating fibroblasts in culture. This drug also has anti-inflammatory and modulating effects on s1p receptors, which may be due to its ability to inhibit the production of proinflammatory cytokines such as tumor necrosis factor alpha (TNFα). 5-bromo-6-methoxy-1H-indole is a potent inhibitor of acid methyl esters, which are involved in inflammation and tissue destruction. 5-bromo-6-methoxy-1H--indole also has an effect on dermal cells, which may be due to its ability to inhibit the production of matrix metalloproteinase enzymes. This drug can also cause atrophy in granuloma cells and prevent the development of inflammatory</p>

<p>Methyl 2-(chloromethyl)nicotinate is an organic compound that belongs to the class of esters. It is a reaction product of methyl 3-hydroxybenzoate and nitrous acid. This compound has antimicrobial activity and can be used to treat bacterial infections. Methyl 2-(chloromethyl)nicotinate has been shown to inhibit the growth of various bacteria, including methicillin-resistant Staphylococcus aureus (MRSA), Escherichia coli, Klebsiella pneumoniae, Pseudomonas aeruginosa, Salmonella typhi, and Salmonella typhimurium. The cyano group in this molecule may be responsible for its antibacterial activity. <br>The efficiency of methyl 2-(chloromethyl)nicotinate varies with different types of bacteria. For example, it was more effective against MRSA than against Escherichia coli or Klebsiella pneumoniae</p>

<p>Versatile small molecule scaffold</p>

<p>(1H-Indazol-4-yl)acetic acid is a cation that has been shown to have pharmacological activity. It is hydrolyzable and is used as an anti-inflammatory agent. This compound also decarboxylates and hydrolyzes, which are processes that produce carboxyl and fluoro groups. (1H-Indazol-4-yl)acetic acid has been shown to be an anti-inflammatory agent, with effects against inflammation in the central nervous system. This drug also inhibits the production of inflammatory cytokines, including tumor necrosis factor alpha (TNFα), interleukin 1β (IL1β), and IL6.</p>

<p>2-Bromo-5-fluoro-4-nitroaniline can be synthesized in a reaction system of ammonium chloride, hydrochloric acid, and water vapor. The reaction is carried out at a temperature of 190°C under reflux. The efficiency of this synthesis is high, and the chemical yield is about 90%.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>2-[[(3aS,4R,6S,6aa)-4-[7-[[(1R,2S)-2-(3,4-Difluorophenyl)cyclopropyl]amino]-5-(propylthio)-3H-[1,2,3]triazolo[4,5-d]pyrimidin-3-yl]- 2,2-dimethyl-tetrahydro-3aH-cyclopenta[d][1,3]dioxol-6-yl]oxy]ethanol-d7 is a compound with brominated sparfloxacin. It has various applications in the field of biochemistry and research chemicals. This compound has been found to have interactions with adipocytes and adipose tissues. Additionally, it has shown potential effects on glycan metabolism and potassium ion channels. Furthermore, this compound has been studied for its potential as an herbicide and its interaction with other substances such as</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Glycidyltrimethylammonium chloride is a quaternary ammonium compound that has been widely used as a disinfectant and in wastewater treatment. It is mainly used to kill bacteria and viruses, although it can also be used to remove hazardous material from water. Glycidyltrimethylammonium chloride has the ability to inhibit bacterial growth by causing cell membrane damage. This compound is also able to inhibit the synthesis of DNA, RNA, and protein in cells by binding to their respective building blocks. In addition, glycidyltrimethylammonium chloride has cytotoxic effects on human cells and significantly inhibits the replication of oral pathogens.</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-Methylbenzo[b]thiophene-2-carboxylic acid (MBTCA) is a heterocyclic compound that is an intermediate in the synthesis of 3-methylthiophene-2-carboxylic acid, a precursor to other drugs. MBTCA is an aerobic, nonpolar compound that has shown antimicrobial activity against some bacteria and fungi. It also has been shown to have practicality as a biomolecular probe for methyl groups in organic solvents. MBTCA can be synthesized by nitration of benzene in the presence of sulfur and sulfoxides. This reaction produces nitrobenzene, which can then be oxidized by potassium permanganate or hydrogen peroxide to produce MBTCA. The most common isomer of MBTCA is 2-(3,5-dimethoxybenzylidene)tetrahydrofuran, with three methyl groups on the</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Methyl 3,3-bis(methylthio)-2-cyanoacrylate is a diphenyl ether that is used as a bactericide. It has been shown to be effective against both Gram-positive and Gram-negative bacteria. Methyl 3,3-bis(methylthio)-2-cyanoacrylate is synthesized by the reaction of malonate with dimethylamine chloride in the presence of hydrochloric acid salt in order to produce chloride ions. The reaction is then heated, which causes the methyl 3,3-bis(methylthio)-2-cyanoacrylate to form. This compound is soluble in organic solvents such as formic acid and can be purified by recrystallization or by distillation.</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>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>1,9-Nonanediol is a chemical substance that has been synthesized with the use of a constant pressure process. It is an asymmetric synthesis with light exposure. The molecule has been characterized by chromatographic methods and has the molecular formula CH3(CH2)9O. 1,9-Nonanediol is a dodecanedioic acid and an aliphatic hydrocarbon. It exists in two forms: one hydroxyl group and one hydrogen bond, which are both involved in the dehydration process. This substance does not have any chloride or magnetic resonance spectroscopy properties because it does not contain any chlorine atoms or hydrogen atoms.</p>

<p>3,6-Dichlorobenzene-1,2-diol is a conjugate acid of benzene. It has two dimensions in the plane of the molecule and three dimensions in space. The molecule is composed of six carbon atoms, six hydrogen atoms, and one chlorine atom. 3,6-Dichlorobenzene-1,2-diol has a centroid at the center of the molecule that is surrounded by a ring of four hydrogen atoms. The hydrogen-bonded molecules stack on top of each other to form a hexagonal shape. 3,6-Dichlorobenzene-1,2-diol forms hydrogen bonds with other molecules through its lone pairs of electrons on both oxygen atoms as well as through its pi electron system.</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-Amino-3-methoxypropanoic acid hydrochloride is a mitochondrial enzyme inhibitor that is used as a research tool to study protein synthesis. It binds to the cytochrome b2 subunit of the mitochondrial respiratory chain, inhibiting the oxidation of pyruvate and affecting the production of ATP. 2-Amino-3-methoxypropanoic acid hydrochloride has been shown to induce apoptosis in human liver cells by triggering caspase 3, which is an important enzyme in the apoptotic pathway. 2-Amino-3-methoxypropanoic acid hydrochloride also has a number of chemical properties that make it useful for analytical chemistry. For example, 2-amino-3-methoxypropanoic acid hydrochloride can be used to measure carboxylic acids, acetylation reactions, hydrogen bonds and hydroxyl groups. It can also be used as a nucle</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>9-Anthracenemethanol is a carcinogenic, mutagenic, and teratogenic compound. It is metabolized by a number of enzymatic reactions, including oxidation by cytochrome P450 enzymes and reduction by glutathione reductase. The compound has been shown to be activated in acid conditions, with an activation energy of 10 kcal/mol. It also forms an acid when heated, which can cause damage to cells. 9-Anthracenemethanol has been shown to have photochemical properties that may be used for the production of dyes or pigments.</p>

<p>1-(Piperazin-1-yl)butan-1-one is a neoplastic cell growth inhibitor that inhibits the proliferation of myeloid, k562 and HL60 cells. It has been shown to inhibit the growth of tumor cells in vitro. 1-(Piperazin-1-yl)butan-1-one is an analog of piperazine, which is known to be a cytotoxic agent with anticancer activity. The mechanism of action is not known, but it may be due to its ability to inhibit DNA synthesis or its inhibition of protein synthesis.</p>

<p>Versatile small molecule scaffold</p>

<p>Iridium(III) bis-(2-phenylpyridine) (Ir{dFCF3ppy}2(bpy)) is a monomeric amido ligand that can be used in polymerization processes. It has an average molecular weight of 185.8 and a transition temperature of -55°C. Ir{dFCF3ppy}2(bpy) is soluble in organic solvents such as chloroform and acetone and will react with amines, anionic sites, and cycloalkyl groups to form polymers. The yields of the polymerization process are dependent on the starting materials used.</p>

<p>Versatile small molecule scaffold</p>

<p>2-(Morpholin-4-yl)acetyl chloride hydrochloride is a fine chemical that is used as a building block for the synthesis of other compounds. It can be used in research and development, or as a reagent. 2-(Morpholin-4-yl)acetyl chloride hydrochloride has high purity and is easily soluble in water. This compound can be used as an intermediate to synthesize other compounds, or it can be used as a scaffold for the formation of complex structures.</p>

<p>Versatile small molecule scaffold</p>