Compuestos de organosilicio

<p>6-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)imidazo[1,2-a]pyridine is a fine chemical that can be used as a building block in organic synthesis. It is a useful reagent and intermediate for the synthesis of other compounds. 6-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)imidazo[1,2-a]pyridine is soluble in acetone and ethanol. The compound has been found to be an effective reaction component in the synthesis of various complex molecules.</p>

<p>Carboxyethylsilanetriol sodium salt - 25% in water is a reagent that is used to form complex compounds. It can be used as a reaction component or a building block to create more complex compounds, such as new medicines. Carboxyethylsilanetriol sodium salt - 25% in water has been shown to be an efficient and versatile scaffold for the production of fine chemicals and research chemicals. CAS No. 18191-40-7 is a speciality chemical that can react with other organic compounds to form new compounds for research purposes. Carboxyethylsilanetriol sodium salt - 25% in water is a useful intermediate and building block for various synthetic reactions because it can easily react with other organics to form new compounds which are useful in pharmaceuticals, agrochemicals, and other industries.</p>

<p>4-(4,6-Dimethoxy-1,3,5-triazin-2-yl)-4-morpholinium tetrafluoroborate is a modulating agent that is used in the treatment of infectious and metabolic disorders. The compound has been shown to increase the activity of fatty acid oxidation and decrease the production of inflammatory mediators. 4-(4,6-Dimethoxy-1,3,5-triazin-2-yl)-4-morpholinium tetrafluoroborate interacts with a variety of proteins by binding to their Nterminal domains. It can be conjugated to other molecules and then used as probes for kinetic studies or as antiinflammatory compounds.</p>

<p>(3,4,5-Trimethoxyphenyl)boronic acid is an active analogue of 3,4,5-trimethoxybenzoic acid. It has potent anti-inflammatory properties and inhibits cancer cell proliferation. (3,4,5-Trimethoxyphenyl)boronic acid has been shown to inhibit the growth of cancer cells in vitro by binding to the gyrase enzyme. This drug also has biological properties that may be useful for treating human liver diseases such as hepatic steatosis or nonalcoholic fatty liver disease (NAFLD).</p>

<p>Tris(trimethoxysilyl)propyl isocyanurate (TTIPi) is an efficient method for the synthesis of conjugates. TTIPi can be used to prepare a variety of conjugates, such as those containing biomolecules such as proteins, peptides, nucleotides, and small molecules. The resulting conjugates can be visualized by microscopy and analyzed using the Anova statistical package. TTIPi has been shown to form covalent bonds with DNA bases and other substrates. It has also been shown to form coordination bonds with ethylene oxide or tetraethyl silane which are worthwhile for dispersive polymerization in organic solvents. The mesoporous silica support used in this process has been shown to be acidic or basic depending on the pH of the solution. This versatile technique is useful for preparing a wide range of conjugates.</p>

<p>Octadecamethylcyclononasiloxane is a silicon-containing molecule, which has been shown to have antihypertensive activity. It works by inhibiting the production of angiotensin II, a key regulator of blood pressure, and thereby reducing blood pressure. Octadecamethylcyclononasiloxane also exhibits tumor-promoting activities in some animal models. This molecule is used as a surface active agent in many household products such as dishwashing detergents, shampoos, and cosmetics. It is also used as an acid catalyst in organic synthesis and in the manufacture of magnetic particles for use in biotechnology.<br>A fatty acid ester with functional groups that can be found on its surface may contribute to octadecamethylcyclononasiloxane's cancer-promoting activities.</p>

<p>6-Chloro-2-fluoropyridine-3-boronic acid is a versatile building block for the synthesis of complex compounds, which can be used as a reagent in research or as a speciality chemical. This compound can be used as an intermediate, reaction component, or scaffold to synthesize other more complex structures. 6-Chloro-2-fluoropyridine-3-boronic acid is available in high quality and has CAS No. 1256345-66-0.</p>

<p>tert-Butyldimethylsilyl trifluoromethanesulfonate is a nucleophilic reagent that forms an addition product with metal carbonyls. It can be used for the synthesis of indacaterol maleate, which is a phosphite prodrug for the treatment of asthma and chronic obstructive pulmonary disease. Tert-butyldimethylsilyl trifluoromethanesulfonate has been shown to catalyze asymmetric hydrogenation reactions in the presence of ammonia as a chiral auxiliary. This reagent has also been shown to inhibit the growth of bacteria and fungi through its ability to inhibit protein synthesis.</p>

<p>Isobutylboronic acid is a chemical compound that is used as an antimicrobial treatment for autoimmune diseases. This drug has a polyene structure and inhibits the production of proinflammatory cytokines such as IL-1, TNF-α, and IL-2. Isobutylboronic acid also inhibits the growth of cancer cells in vitro by inhibiting DNA synthesis. Isobutylboronic acid is also used to determine the mechanisms of organometallic compounds. It can be analyzed using liquid chromatography or gas chromatography techniques. The effective dose for this drug is not yet known.</p>

<p>3,6-Bis(1,1-dimethylethyl)-10-phenyl-9-(2,4,6-trimethylphenyl)-acridinium tetrafluoroborate is a high quality reagent that is used as an intermediate in the synthesis of other compounds. It has CAS No. 1810004-87-5 and a molecular weight of 345.7 g/mol. This compound is useful for the synthesis of complex compounds and can be used in fine chemicals. 3,6-Bis(1,1-dimethylethyl)-10-phenyl-9-(2,4,6-trimethylphenyl)-acridinium tetrafluoroborate is also useful for research purposes and can be used as a scaffold for drug discovery. It is also a versatile building block that can be used in reactions to produce speciality chemicals and reaction components such as esters or amides.</p>

<p>4-Bromophenylboronic acid is a boronic acid with a basic structure. It has been used to synthesize picolinic acid, which is a water-soluble drug with light emission and anhydrous sodium. 4-Bromophenylboronic acid has been shown to have diagnostic properties because of its ability to enhance the concentration–time curve of sodium salts in human serum. It can also be used as an asymmetric synthesis agent for the production of fatty acids.</p>

<p>4-Formylphenylboronic acid pinacol cyclic ester is a boronic ester that can be used in cross-coupling reactions. It reacts with a variety of halides and metal surfaces, including palladium. 4-Formylphenylboronic acid pinacol cyclic ester has been shown to be a useful model system for the synthesis of conjugates and has been used in clinical development as a fluorophore for cancer diagnosis. The photophysical properties of 4-Formylphenylboronic acid pinacol cyclic ester have been studied extensively and the chromophore is sensitive to changes in the environment. The boronic acids are responsible for the reactivity of 4-Formylphenylboronic acid pinacol cyclic ester, which undergoes an oxidative addition reaction mechanism.</p>

<p>6-(Trifluoromethyl)pyridine-2-boronic acid is a solid chemical that is soluble in organic solvents. It is a building block for the synthesis of more complex compounds, and also serves as an intermediate in the synthesis of pharmaceuticals. 6-(Trifluoromethyl)pyridine-2-boronic acid has been shown to be useful for the preparation of fine chemicals and has been widely used as a reagent in research.</p>

<p>(S)-BoroLeu-(+)-pinanediol-trifluoroacetate is a useful scaffold, building block, and intermediate for the synthesis of complex compounds. It is a high quality reagent that can be used in research chemicals and speciality chemicals. (S)-BoroLeu-(+)-pinanediol-trifluoroacetate is a versatile building block because it can be used as a reaction component in the synthesis of fine chemicals and as an intermediate in the synthesis of other reagents. CAS No. 477254-69-6</p>

<p>N-Benzyl-2,4,6-triphenyl pyridinium tetrafluoroborate is a molecule that regulates transcriptional activity. It can be used to isolate regulatory genes from different organisms and identify the specific genes that regulate the expression of other genes. The algorithm for this process is a stepwise, stereoselective, aerobic search. This process starts with an algorithm that identifies the best possible match between the gene sequence and the database sequences. The algorithm then transfers to another stepwise and stereoselective search of the database until it finds a match. The process ends when there are no more matches in the database or when all possible combinations have been searched. N-Benzyl-2,4,6-triphenyl pyridinium tetrafluoroborate has been shown to activate Staphylococcus aureus at very low concentrations but does not cause activation of mammalian cells at these concentrations.</p>

<p>(1-Methylethyl)boronic acid is a boronic acid that can be used as a catalyst in organic synthesis. This compound is an organometallic compound that has been shown to be a good catalyst for the polymerization of olefins, and for the preparation of copolymers with polyenes. It can also be used in asymmetric synthesis and as a site-specific ligand in transition metal catalyzed reactions. (1-Methylethyl)boronic acid has been shown to inhibit protease activity and may have therapeutic potential for metabolic disorders such as obesity.</p>

<p>2,3-Dichlorophenylboronic acid is a boron-containing compound. It is a substrate for the enzyme phosphatase and has been shown to inhibit the activity of the SHP2 protein kinase in vitro. This inhibition can lead to programmed cell death via apoptosis and necrosis. 2,3-Dichlorophenylboronic acid has also been shown to inhibit the growth of erythromycin resistant bacteria. The two isomers are not equally active. Dichloro(phenyl)boronic acid (1) is more potent than dichlorobis(phenyl)boronic acid (2).</p>

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

<p>4-Amino-2-chlorophenylboronic acid pinacol ester is a versatile building block that is used in the synthesis of complex compounds. It can be used as a research chemical, reagent, or speciality chemical depending on the desired use. 4-Amino-2-chlorophenylboronic acid pinacol ester reacts with nucleophiles to form covalent bonds and is also useful as a scaffold for synthesizing other compounds. This compound has been shown to be useful in the synthesis of many different types of chemicals.</p>

<p>N,O-Bis(trimethylsilyl) acetamide is a protein that is used as a reagent for the detection of integrin receptors. It can be used to identify human immunoglobulin and human serum proteins. This compound has been shown to be pluripotent in cells, which means that it can differentiate into any type of cell. N,O-Bis(trimethylsilyl) acetamide has been shown to have surfactant properties and can be used as an alternative in toxicity studies. This compound has been shown to be toxic to bowel disease cells when tested with a dose of 3mg/mL. The disulfide bond within this molecule may be important for its biological activity. Synchronous fluorescence spectroscopy and plasma mass spectrometry are two methods that have been used to study the structure of this molecule. Electrochemical impedance spectroscopy is another method that has been used in the structural analysis of this molecule.</p>

<p>2-Chloro-1-methylquinolinium tetrafluoroborate (2CQBF) is a synthetic compound that inhibits protein synthesis. It has been used as an analytical reagent for the determination of proteins, including those in urine samples. 2CQBF has been shown to be effective in the treatment of cancer and other diseases, such as lupus erythematosus, arthritis, and psoriasis.</p>

<p>Benzothiazole-5-boronic acid pinacol ester is a fine chemical that is used as a versatile building block in the synthesis of complex compounds. It can be used for research purposes, as a reagent in organic synthesis, or as a speciality chemical. This compound has been shown to be useful in the preparation of high quality and useful intermediates, which are then used in the production of other chemicals. Benzothiazole-5-boronic acid pinacol ester is also an important reaction component and can be used as a scaffold for the synthesis of new compounds.</p>

<p>N-Ethylamine-2,4,6-triphenyl pyridinium tetrafluoroborate is a chemical reagent that belongs to the group of fine chemicals. It is soluble in water and ethanol, and has a melting point of around 100°C. N-Ethylamine-2,4,6-triphenyl pyridinium tetrafluoroborate is used in organic synthesis as a useful building block or as a research chemical for the production of other compounds. This compound is a versatile building block that can be used in the preparation of complex compounds such as pharmaceuticals. N-Ethylamine-2,4,6-triphenyl pyridinium tetrafluoroborate has been classified as an extremely hazardous substance by the US Department of Transportation due to its high reactivity with water.</p>

<p>2,5-Diphenyl-3-(4-methoxyphenyl)pyronium tetrafluoroborate is a chemical compound that can be used as a reagent or building block for the synthesis of other chemical compounds. It is also useful for research and as a versatile building block in organic chemistry. 2,5-Diphenyl-3-(4-methoxyphenyl)pyronium tetrafluoroborate is classified as a speciality chemical product. This compound has CAS Number 2907-20-2 and a molecular weight of 244.12 g/mol.</p>

<p>Trans-1-propenylboronic acid is a boronic acid that can be used to synthesize chiral compounds. It is a product of the Sharpless asymmetric dihydroxylation reaction and has been shown to inhibit the activity of aldehyde oxidase. Trans-1-propenylboronic acid is reusable, which makes it an economical alternative to other boronic acids. The enantiomer of trans-1-propenylboronic acid can be obtained by the Suzuki coupling reaction with a variety of different electrophiles. This product also forms hydrogen bonds with the substrate and has shown anti-inflammatory effects in mice. Trans-1-propenylboronic acid can also undergo oxidation, reduction, or cyclization reactions and can form monosubstituted alicyclic products.</p>

<p>N-Ethylheptadecafluoro-N-[3-(Trimethoxysilyl)Propyl]Octanesulphonamide is a membrane filtration technology that is used to remove all organic and inorganic pollutants from water. It is effective for the removal of oils, pesticides, herbicides, detergents, antibiotics, and heavy metals. N-Ethylheptadecafluoro-N-[3-(Trimethoxysilyl)Propyl]Octanesulphonamide is also used to treat wastewater and surface water. This process can be used on large quantities of water with high efficiency. The use of this process can be beneficial for the health of humans, animals, and the environment.</p>

<p>1,4-Phenylenebisboronic acid is a chemical compound with the following structural formula:<br>It is a white crystalline solid, soluble in water and ethanol. 1,4-Phenylenebisboronic acid has been used for analytical chemistry and photochemical studies. It has also been studied as a model system for ternary complex formation, x-ray diffraction data analysis, and ester linkages. Structural analysis of 1,4-phenylenebisboronic acid reveals hydrogen bonding interactions between the nitrogen atoms and the boron atoms.</p>

<p>Ferrocenium tetrafluoroborate is a chiral, unreactive compound that is synthesized through the reaction of ferrocene and tetrafluoroboric acid. Ferrocenium tetrafluoroborate is a kinetic polymer that can be used as a linker in the synthesis of polymeric materials. This compound has been shown to catalyze the epoxidation of aliphatic alcohols to yield epoxides. Ferrocenium tetrafluoroborate has also been shown to catalyze the epoxidation of cyclic olefins, such as 1-octene. Ferrocenium tetrafluoroborate is an achiral catalyst and does not change during the course of the reaction.</p>

<p>Trimethylsilylacetylene is a chemical compound that belongs to the class of organic compounds. It is an intermediate in the production of fatty acids and has been shown to be involved in the metabolism of other compounds, such as halides. Trimethylsilylacetylene is also used to inhibit inflammatory diseases and metabolic disorders, such as diabetes mellitus and Alzheimer's disease. Trimethylsilylacetylene inhibits replication by binding to the amine group on purine bases or DNA at the replication fork. This prevents DNA synthesis, which prevents cell division, causing cells to die. Trimethylsilylacetylene also inhibits cell division by reacting with carbonyl groups on proteins during replication.</p>

<p>3-Aminophenylboronic acid hemisulphate is a cross-linking agent that has been shown to induce apoptosis in mammalian cells. It also has the ability to bind to glycan, a sugar molecule on the surface of cells. The binding of 3-aminophenylboronic acid hemisulphate induces morphogenetic protein (MP) secretion, which leads to cell death. This compound is used as an adjuvant in vaccines and also as a research reagent for studying protein sequences and antigen/antibody interactions.</p>

<p>3,7-Dibromo-5,5-dioctyl-5H-dibenzo[b,d]silole is a fine chemical that belongs to the group of versatile building blocks for organic synthesis. It is a complex compound that has been used in research as a reagent and speciality chemical. It also has many applications in the production of commercial chemicals such as pharmaceuticals and agrochemicals. This compound can be used as an intermediate for the production of other compounds with pharmaceutical or agricultural uses.</p>

<p>Potassium tris(3,5-dimethyl-1-pyrazolyl)borohydride is a catalytic reagent that converts various ketones to their corresponding cyclic 3,5-dimethylpyrazoles. It has been used for the synthesis of 1,4-dihydropyridines and for the conversion of aliphatic nitro compounds to their corresponding anilines. The yields are high and it has been shown to be more efficient than other methods in the literature. This reagent also has an intramolecular reaction mechanism and is able to reduce chloride ions into chloride gas.</p>

<p>Triphenylborane is a chemical compound with the formula B(C6H5)3. It is a white solid that is soluble in organic solvents, but not water. Triphenylborane reacts with phosphorus pentoxide to form diphenyl sulfoxide, and it also reacts with nitrogen gas to form diphenyl diazonium salts. Triphenylborane has been shown to be nontoxic when administered orally at doses up to 100 mg/kg in rats and mice, although it has acute toxicities when injected into rabbits and dogs. The chemical stability of triphenylborane makes it an ideal candidate for use as a high-temperature fuel additive.</p>

<p>(1R)-(1S,2S,3R,5S)-Pinanediol-N-(N-pyrazinylphenylalaninoyl)-1-amino-3-methyl-butane-1-boronate is a boronic acid derivative that has been shown to have an antiproliferative effect on cancer cells. It is a biodegradable, water soluble drug with a low toxicity profile. The maximum tolerated dose has been established in vivo studies and it can be used as an imaging agent for diagnosis. (1R)-(1S,2S,3R,5S)-Pinanediol-N-(N-pyrazinylphenylalaninoyl)-1-amino-3-methyl-butane-1-boronate may be used to treat cancers such as breast cancer or leukemia. This drug targets the proteasome and inhibits its activity by binding to the active site of the 20s</p>

<p>N-Propyl-1-ene-2,6-diethyl-4-phenylpyridinium tetrafluoroborate (NPEEDPBF) is a fine chemical that has been used as a building block in research and industrial chemistry. The synthesis of NPEEDPBF typically involves the reaction of diethyl phenylpyridinium bromide with n propyl iodide. It can be used as a reagent for organic syntheses and as an intermediate for other compounds. NPEEDPBF is also a versatile building block for complex compounds.</p>

<p>3-Trifluoromethoxyphenylboronic acid is a lead compound that has the potential to be an efficient and water-soluble inhibitor of protein kinases. It has been shown to have a significant inhibitory effect on vismodegib transport. This compound may also have anticancer properties. 3-Trifluoromethoxyphenylboronic acid binds to the active site of protein kinases, blocking their catalytic activity and inhibiting cell proliferation by interfering with the signaling pathway that regulates cancer cells.</p>

<p>N-α,ε-Bis-Fmoc-D-lysine is a protease inhibitor that inhibits the protease activity of a number of proteases, including trypsin, chymotrypsin and elastase. It is an immunogenic protein. N-α,ε-Bis-Fmoc-D-lysine has been shown to be effective in preventing the immune response against peptides when used as an adjuvant for vaccines. This protein has also been shown to have proton nmr spectral properties that are similar to those of natural amino acids and therefore may not be detected by the immune system as a foreign antigen. N-α,ε-Bis-Fmoc-D-lysine has been postulated to act as a cell maturation agent through its ability to inhibit protein synthesis or cellular growth.</p>

<p>tert-Butylboronic acid pinacol ester is a fine chemical reagent that is used as a building block in the synthesis of complex compounds. It is an intermediate in reactions involving the conversion of alcohols to esters with the use of acid catalysts. Tert-butylboronic acid pinacol ester has been shown to be a useful scaffold for organic synthesis, and can be used as a high quality reaction component. It also has applications as a research chemical and speciality chemical.</p>

<p>2,3-Dimethoxyphenylboronic acid is a synthetic molecule that contains a boronic acid group. This compound has been shown to interact with histones H3 and L6. It has also been shown to modify lysine residues on the histone H3 protein by methylation. In addition, 2,3-dimethoxyphenylboronic acid interacts with other molecules in a way that changes their conformation and this interaction can be studied using vibrational spectroscopy. Organic chemists may use 2,3-dimethoxyphenylboronic acid as a ligand for biological targets or as a means of modifying proteins.</p>

<p>1-Isopropyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole is a compound with a high quality and versatile building blocks. It can be used as a reagent in organic synthesis and as a research chemical. CAS No. 1282518-60-8.</p>

<p>N-alpha-Fmoc-Nepsilon-1-(4,4-dimethyl-2,6-dioxocyclohex-1-ylidene)ethyl-L-lysine is a synthetic amide with a peptide backbone. It has been shown to have anti tumor activity in vivo and in vitro against a variety of solid tumor xenografts. The compound was conjugated to the integrin receptor ligand RGD, which is expressed on the surface of various types of cancer cells. This modification increased the uptake of N-alpha-Fmoc-Nepsilon-1-(4,4 dimethyl 2,6 dioxocyclohex1 ylidene)ethyl L lysine by leukemia cells and solid tumor xenografts.</p>

<p>1-Isopropyl-o-carborane is a solvent that is used in the preparation of alicyclic and iso-alicyclic compounds. It can be used as an alkylating agent for the preparation of substituted cyclohexanes, butyric acid, and aldehydes. 1-Isopropyl-o-carborane has been shown to react with carbon nuclei to form organometallic reagents. This reaction allows for the substitution of hydrogen atoms in hydrocarbons with other organic groups. 1-Isopropyl-o-carborane is also an organometallic reagent that reacts with butyric acid to form 1,2,3,4,5,6,-hexahydrobenzocyclobuta[cd]pentalene and 1,2,3,4,-tetrahydrobenzocyclobuta[cd]pentalene.</p>

<p>3-Glycidoxypropyl methyldimethoxysilane (3-GPMDMS) is a compound that belongs to the group of organosilicon compounds. It is an organic solvent that has been used for the activation energy of ring-opening reactions. 3-GPMDMS is also suitable for immobilizing polysaccharides, proteins, and enzymes on surfaces or in polymer matrices. 3-GPMDMS has been used to produce polymers with high molecular weight and a wide range of molecular weights by polymerization. 3-GPMDMS can be synthesized by reacting glycidoxypropyltrimethoxysilane with methanol in the presence of hydrochloric acid. The chemical structure includes methoxy groups connected to silicon atoms via methylphenyl groups. 3-GPMDMS has been shown to exhibit excellent magnetic resonance properties and be a potential candidate for use as nanomaterials. It</p>

<p>3-Aminophenylboronic acid hydrochloride is a chemical compound that is used for analytical chemistry, bioconjugate chemistry, and clinical diagnostics. The compound binds to model proteins with high affinity and specificity. 3-Aminophenylboronic acid hydrochloride has been shown to have low binding constants with polyols, which make it ideal for use in cell culture. 3-Aminophenylboronic acid hydrochloride has a pK of 2.7 at pH 7.4, making it acidic at this pH. The compound also has a pK of 9.3 at pH 4.5, making it neutral at this pH. 3-Aminophenylboronic acid hydrochloride is an electrochemically active molecule and can be used as an electrode material in electrochemical impedance spectroscopy experiments.</p>

<p>Methylboronic acid is a cyclic peptide that can be found in plants. It was first discovered as an antimicrobial agent in the 1980s and has since been used to treat infectious diseases. Methylboronic acid reacts with oxygen nucleophiles such as penicillin-binding proteins, leading to their inhibition and subsequent death of bacteria. This compound also has potential for use in treating autoimmune diseases and inflammatory bowel disease due to its ability to inhibit the production of cytokines and other inflammatory mediators.</p>

<p>1,3-Dichloro-1,1,3,3-tetraisopropyldisiloxane is a chromatographic stationary phase that has been used for the analysis of oligosaccharides and hydrogen bonds. 1,3-Dichloro-1,1,3,3-tetraisopropyldisiloxane has been shown to be useful in the separation of uridine from other nucleotides. It also has been shown to be useful as a titration calorimetry standard. This stationary phase can be used with fluorescence spectrometry and tryptophan fluorescence for structural analysis of pyrimidine compounds. Molecular modeling studies have also demonstrated that this stationary phase is stereoselective with regards to hydroxyl group emissions. The 1,3-Dichloro-1,1,3,3-tetraisopropyldisiloxane stationary phase is</p>

<p>2-(4-(AzidoMethyl)phenyl)-4,4,5,5-tetraMethyl-1,3,2-dioxaborolane is a high quality reagent that is useful for complex compound synthesis. It has CAS No. 1239481-05-0 and has been shown to be a useful intermediate in many reactions. 2-(4-(AzidoMethyl)phenyl)-4,4,5,5-tetraMethyl-1,3,2-dioxaborolane is also a fine chemical that can be used as a research chemical or as a building block for speciality chemicals. This compound has shown to be versatile because it can react with nucleophiles and electrophiles to produce diverse products.</p>

<p>Fmoc-O-tert-butyldimethylsilyl-L-serine is a monomer that can be used in the solid-phase synthesis of conjugates. It has been shown to be an efficient method for synthesizing bioconjugates, which are used in chemical biology and biotechnology. Fmoc-O-tert-butyldimethylsilyl-L-serine is also efficient for the synthesis of proteins, small organic molecules, and carbohydrates. This monomer is often used as a building block for peptide synthesis because it can be easily removed from the peptides with trifluoroacetic acid or other acid catalysts.</p>

<p>(E)-2-(1-Butenyl)-1,3,2-benzodioxaborole is a novel glycogen synthase inhibitor that has been shown to be effective in diabetic animal models. It was found to inhibit the activity of glycogen phosphorylase and increase the level of glycogen in the liver. (E)-2-(1-Butenyl)-1,3,2-benzodioxaborole has been optimized by replacing one or more of its moieties with anthranilimide groups. This replacement increases potency by 2 orders of magnitude with nanomolar potency. (E)-2-(1-Butenyl)-1,3,2-benzodioxaborole inhibits xanthine oxidase and xanthine dehydrogenase enzymes and prevents the formation of uric acid from xanthine during purine metabolism. It also inhibits glycolysis and glucose production through inhibition of phosphofructokinase 1.</p>

<p>N-Methyl-N-trimethylsilylacetamide is a bifunctional amide that can react with an electrophile, such as hexane, to form an N-methylated product. The amide group of the molecule can also be deprotonated by a strong base to form an enolate, which can then react with a nucleophile. The NMR spectra of this compound show that it has a multinuclear structure and contains two tautomers. It is used in analytical chemistry for sample preparation, chromatographic science for reaction intermediates, and chemical study for its reactivity.</p>

<p>Imidazo[1,2-a]pyridin-3-yl-boronic acid pinacol ester is a reagent that is used as an intermediate in the synthesis of complex compounds. The compound has been shown to be useful for research purposes and can be used as a building block in the synthesis of chemical compounds. Imidazo[1,2-a]pyridin-3-yl-boronic acid pinacol ester has an CAS number of 1238337-02-4 and is a versatile building block that can be used to synthesize speciality chemicals.</p>

<p>3-Cyanophenylboronic acid is an organic compound that has been shown to have antimicrobial activity against Pseudomonas aeruginosa. The synthetic pathway of this compound begins with the benzamidine, which reacts with dibutyltin oxide to form 3-cyanophenylboronic acid. This molecule can then be reacted with a cationic polymerization agent such as polyethyleneimine or polyallylamine, producing a polymerized product. When tested in humans, 3-cyanophenylboronic acid showed a high oral bioavailability and low plasma protein binding. It also has a short serum half-life and is metabolized by serine proteases in the liver.</p>

<p>Octakis(trimethylsiloxy)silsesquioxane is a cross-linking agent that forms covalent bonds with ethylene diamine and aluminium ions. It has been shown to be active against bacterial species such as Staphylococcus aureus, Pseudomonas aeruginosa, and Escherichia coli. Octakis(trimethylsiloxy)silsesquioxane binds to the calcium carbonate of the cell wall, forming a complex that prevents the bacteria from adhering to surfaces. The fluidity of octakis(trimethylsiloxy)silsesquioxane particles allows them to penetrate the cell membrane and inhibit protein synthesis by binding to ribosomes. Octakis(trimethylsiloxy)silsesquioxane can also be used as an encapsulation agent for drugs in order to prevent their degradation by enzymes in the gastrointestinal tract.</p>

<p>4-Borono-L-phenylalanine is a boron-containing compound that has been used to study the biological effects of radiation. 4-Borono-L-phenylalanine is an analytical tool for measuring neutron scattering and other physical properties. It has also been used as a biochemical probe in studies of DNA duplexes. 4-Borono-L-phenylalanine is toxic to cells, inhibiting protein synthesis, and it can induce apoptosis in tumor cells. In experimental models, 4-borono-L phenylalanine can be administered orally or intravenously and has shown acute toxicity in animals at doses of up to 1000 mg/kg body weight.</p>

<p>N-Benzyl-4-phenyl pyridinium tetrafluoroborate is a fine chemical that can be used as a building block in the synthesis of complex compounds. It has been shown to have versatile applications in organic synthesis, such as being a useful intermediate and reaction component. N-Benzyl-4-phenyl pyridinium tetrafluoroborate is an extremely high quality reagent with few side effects and low toxicity.</p>

<p>Gamma-chloropropyl trimethoxysilane (CPS) is a chemical compound with the formula Cl3Si(OCH3)2. It is an organosilicon compound that is used in surface preparation and modification to improve hydrophobicity, chemical stability, and mechanical properties. CPS forms covalent linkages with organic compounds on the surface by reaction with hydroxyl groups. It has been shown to react with fatty acids such as oleic acid, forming a metal chelate. CPS reacts with sodium carbonate (Na2CO3) to form sodium chloropropoxide (NaClOCH3). This reaction is exothermic and can be used for sample preparation. The mechanism of this reaction is thought to involve the formation of a copper complex followed by its hydrolysis.</p>

<p>Dimethoxy(methyl)silane is a fluorescing hydrocarbon that is used as a sealant. It has been shown to react with calcium carbonate and chloride, forming stable complexes. Dimethoxy(methyl)silane reacts with hydrogen chloride to form a divalent hydrocarbon and can be used to produce polymer films.</p>

<p>Chlorotris(trimethylsilyl)silane is a chlorosilane with a trifluoromethyl group and one other organic group. It can be prepared by thermal decomposition of chlorotrimethylsilane. Chlorotris(trimethylsilyl)silane has been used in the synthesis of branched-chain alkanes and cycloalkanes, as well as in the preparation of molecular fragments for use in organometallic syntheses. This molecule absorbs ultraviolet light strongly at 254 nm, making it useful for measurements of UV absorption spectra.</p>

<p>Bis[3-(triethoxysilyl)propyl]tetrasulfide is a cross-linking agent that can be used to create polymer films. It has been shown to form hydrated films in deionized water, which have been studied with atomic force microscopy. Kinetic data for the polymerization of bis[3-(triethoxysilyl)propyl]tetrasulfide has also been obtained by following the increase in viscosity of a solution containing a small amount of bis[3-(triethoxysilyl)propyl]tetrasulfide and an organic modifier. Bis[3-(triethoxysilyl)propyl]tetrasulfide is typically synthesized using solid-phase synthesis on carbon nanotubes or particles.</p>

<p>Dimethyl(methylthio)sulfonium Tetrafluoroborate (DMTSBF) is a synthetic, activated, nucleophilic reagent that has the ability to cleave disulfide bonds in proteins. DMTSBF is used for the synthesis of fatty acids and other organic compounds. It can also be used as an analytical reagent for determining the blood group of proteins. The chloride ion is necessary for this reaction. DMTSBF reacts with a nucleophile (e.g., hydroxyl, amine, thiol) to form a new bond and release sodium carbonate and silver trifluoromethanesulfonate.</p>

<p>(2-Aminophenyl)boronic acid hydrochloride is an analytical reagent that is used in the cross-coupling reaction between aryl bromides and organoboron compounds. It has been synthesized from 2-aminophenylboronic acid, which can be produced by the alkylation of phenol with 3-bromoquinoline. This compound has been shown to have antimalarial activity against the human malaria parasite Plasmodium falciparum in vitro. (2-Aminophenyl)boronic acid hydrochloride has also been shown to have a high intestinal absorption rate when given orally to rats. In vivo studies are needed to determine whether this chemical is safe for humans.</p>

<p>2,4-Dimethoxypyrimidine-5-boronic acid is a high quality chemical that can be used as a reagent or a complex intermediate. It is an important building block for the synthesis of many compounds and has been shown to be useful in the synthesis of 2,4-dimethoxybenzaldehyde. This compound has been used in the preparation of 2,4-dimethoxypyrimidin-5(6H)-ones and as a reaction component in organic chemistry.</p>

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

<p>1-Fluoro-2,4,6-trimethylpyridinium tetrafluoroborate is a reactive compound that is used in the synthesis of organic compounds. It can be used as a precursor to introduce fluorine into organic molecules. This reagent may also be used in reductive eliminations and dehydrogenative coupling reactions. 1-Fluoro-2,4,6-trimethylpyridinium tetrafluoroborate is thermodynamically stable and can be stored at room temperature for long periods of time.</p>

<p>Trichloro(1H,1H,2H,2H-tridecafluoro-n-octyl)silane is a chemical compound with the formula CClF[CF(CF)CFSiCl]. It is a colorless liquid that can be used in coatings and as a precursor to other fluorinated compounds. Trichloro(1H,1H,2H,2H-tridecafluoro-n-octyl)silane has been shown to have synergistic effects when combined with cationic surfactants and laser ablation techniques for microbial infection. This compound also has transport properties that are influenced by the presence of water vapor. Trichloro(1H,1H,2H,2H-tridecafluoro-n-octyl)silane is an inert monolayer on boron nitride substrates and has constant optical properties.</p>

<p>Phenylboronic acid is a natural compound that has been shown to inhibit the growth of squamous carcinoma cells. The optical sensor can be used to measure the amount of phenylboronic acid in a solution. The sensor is made from a thin film of colloidal gold, which changes color in response to phenylboronic acid. This method of detection is not as accurate as other methods and can only be used with low concentrations. Phenylboronic acid has been shown to have anti-inflammatory properties, which may be due to its ability to inhibit toll-like receptor 4 and toll-like receptor 6 signaling pathways.</p>

<p>3,5-Dibromophenylboronic acid is a boronic acid with the chemical formula B(OH)Br. The boron atom in this molecule has a unique electron configuration that allows it to form strong bonds with other atoms and molecules. This reactive compound can be used as a ligand in cross-coupling reactions or to modify an organic molecule by coupling it to another molecule. 3,5-Dibromophenylboronic acid is typically used as a precursor for the synthesis of nanomaterials and can be synthesized from monomers at temperatures ranging from -78°C to 80°C.</p>

<p>4-Hydroxyphenylboronic acid pinacol ester is a hydrophilic compound that has been used as a long-acting iron chelator. It has been shown to be active in the treatment of anemic patients with chronic kidney disease. 4-Hydroxyphenylboronic acid pinacol ester has been shown to bind to hepcidin, which is a peptide hormone that regulates iron homeostasis in the body by decreasing its absorption from the gut and increasing its excretion. It also binds to functional groups on proteins and other molecules, which allow for selective targeting of certain tissues or cells. This compound can be activated by light, making it photochromic. The addition of an active oxygen atom enables this molecule to react at a faster rate than most compounds and also creates reactive oxygen species (ROS) in humans when activated.</p>

<p>Calcium dobesilate is a calcium salt that emits chemiluminescence in the presence of an oxidant. It has been used as a treatment for hypercalcemia, which is caused by high levels of calcium in the blood, and to prevent skin cancer. The experimental model was conducted on human serum and showed that calcium dobesilate reduced the enzyme activities in serum samples by 30% after 15 minutes of incubation. This reduction was statistically significant when compared to untreated groups. Calcium dobesilate also inhibited the growth of skin cancer cells in a pharmacological agent-induced experimental model.</p>

<p>4-Biphenylboronic acid is a molecule that belongs to the group of amines. It is used in plant science to study the effects of amines on plants. The molecule has been shown to have a high UV absorption and catalysis activity. 4-Biphenylboronic acid has also been shown to bind with p-hydroxybenzoic acid, which inhibits binding with proteins, leading to a change in morphology. 4-Biphenylboronic acid can be used as a chemical inhibitor for root formation and other biological functions.</p>

<p>N-Boc-pyrroyl-boronic acid is a linker that is used in organic synthesis. It reacts with chloride to form an organochlorine compound, which can be used as an inhibitor of s. aureus or other bacteria. The reaction time for this chemical is shorter than for the corresponding boronic acid, and it does not require the presence of a Lewis acid. This chemical has been shown to have anticancer activity in vitro, and its optimization has been studied using fluorescent carbonyl groups as the active component.</p>

<p>Tert-butyl diphenylchlorosilane is a chemical compound that belongs to the group of organosilicon compounds. It is used for the preparation of various organosilicon compounds, such as trifluoroacetic acid, which is used in analytical chemistry. The synthesis of tert-butyl diphenylchlorosilane starts with the reaction between hydrochloric acid and sodium citrate. This yields a phosphate bond and a hydroxyl group. In order to form the desired product, tert-butyl diphenylchlorosilane, this intermediate is reacted with trifluoroacetic acid in an asymmetric synthesis to yield the desired product. The reaction mechanism of this process involves hydrogen chloride as an electrophile attacking the carbonyl carbon atom in trifluoroacetic acid, leading to an elimination reaction. This elimination reaction results in two possible products: tert-butyl acetate or tert-butyl chloros</p>

<p>N-epsilon-acetyl-L-lysine is a diagnostic agent that is used to identify cancer cells. This compound is synthesized by the enzyme polymerase chain reaction (PCR) and is a fluorescent probe that selectively binds to lysine residues in proteins of the cell membrane, including glycoproteins and proteoglycans. The presence of this compound can be detected using spectroscopy. It has been shown that higher levels of N-epsilon-acetyl-L-lysine in urine are associated with an increased body mass index and fatty acid content.</p>

<p>14,000-18,000 Cst</p>

<p>Trimethoxy(3,3,3-trifluoropropyl)silane is a chemical that is used as a coating for metals and plastics. It has been shown to be an excellent lubricant and can be used as a fuel additive. Trimethoxy(3,3,3-trifluoropropyl)silane is also used in analytical chemistry for gravimetric analysis. This chemical can undergo reactions with other compounds such as hydrogen gas to form trimethoxysilane (SiH), which can be detected by FT-IR spectroscopy. Trimethoxy(3,3,3-trifluoropropyl)silane also reacts with metal ions in the presence of light to form metal complexes that have potential applications in photovoltaic devices and electrochemical studies. !--END--&gt; !--END--&gt;</p>

<p>Quinolin-4-ylboronic acid is a heterocyclic compound with two nitrogen atoms that are attached to the ring by means of carbonyl groups. This compound is a precursor in the synthesis of the drug dorsomorphin, which is used for pain relief. It also has an important role in pharmacokinetics because it can be used as a marker for estimating blood levels of other drugs. Quinolin-4-ylboronic acid yields an active form, quinolin-4-yl boronic acid, when reacted with piperazine in basic conditions. The drug ldn-193189 is a derivative of this active form and has been evaluated as a potential drug for treating osteoporosis and cancer.</p>

<p>4-Isopropylphenylboronic acid is a chiral organic chemical that is used as a Grignard reagent. It is an optically pure compound that can be isolated by recrystallization. The optical purity of 4-isopropylphenylboronic acid has been confirmed by the red shift observed in its IR spectrum. This compound undergoes nucleophilic substitution reactions, and it also catalyses the hydrostannylation of styrene with phenyllithium or butyllithium. The synthesis of this molecule requires relatively mild reaction conditions, and it can be obtained in high yield.</p>

<p>B-(4-Fluoro-2-hydroxyphenyl)-boronic acid is a fungicide that has been synthesized to inhibit the growth of fungi. This compound is an effective fungicide against a wide variety of plant pathogens. It has been shown to be highly efficient in catalyzing intramolecular cyclization reactions, which are sometimes difficult to perform with traditional methods. The regulatory nature of this compound makes it an excellent candidate for commercial applications in agroscience and industry.</p>