Composés organosiliciés

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

<p>Iron bis(tetrafluoroborate) hexahydrate is a ferrimagnetic, thermally stable coordination compound that has been shown to interact with bidentate ligands. Iron bis(tetrafluoroborate) hexahydrate can be used as a mononuclear section in analogy to the octahedral section of nickel bis(tetrafluoroborate) hexahydrate. The ligands are methyl groups, which are diffracted at 2θ values of 12.8° and 18.3°. The compound is stable in solvents such as dimethylsulfoxide and tetrahydrofuran. It also has chelate ligand transfer properties, which are due to the presence of two hydroxyl groups on each iron atom.</p>

<p>Bis (1,5-Cyclooctadiene) rhodium(I)tetrafluoroborate (BODIPY) is a catalyst that enhances the rate of hydrosilylation reactions. This catalyst has been shown to be effective in the synthesis of aryl chlorides from amines and aldehydes with high enantioselectivity. BODIPY is also immobilized on silica gel to create an active catalyst for asymmetric synthesis. The immobilization process on silica gel is done by reacting BODIPY with ammonium formate and amines. The resulting catalyst can be used for the synthesis of functionalized organic compounds, such as pyrrolidines, tetrahydrofurans, and thiophenes.</p>

<p>Azidotrimethylsilane is a chemical compound that can be used in various reactions. It is an unsymmetrical compound with the molecular formula of CH3SiN3, and has an asymmetric carbon atom with four different substituents. Azidotrimethylsilane reacts with nucleophiles to form azides, which can be used as antiviral agents or to synthesize other compounds. It also participates in transfer reactions, such as the reaction of trifluoroacetic acid and fatty acids to form esters. The hydroxyl group on the silicon atom increases its reactivity because it can act as a nucleophile in addition to its electrophilic properties. !-- --&gt;Azidotrimethylsilane is an unsymmetrical compound with the molecular formula CH3SiN3, and has an asymmetric carbon atom with four different substituents. Azidotrimethylsilane reacts with nucleophiles to form az</p>

<p>1-Hexyl-o-carborane is a human bioassay that has shown carcinogenic activity. It has been observed to cause cancer in humans through its ability to bind to DNA and alter the cell cycle. 1-Hexyl-o-carborane is an organometallic compound that binds to ferrocene and other organometallic compounds, preventing their use as anticancer drugs. 1-Hexyl-o-carborane can be synthesized by reacting hexylmagnesium bromide with ammonium carbonyl chloride in a one pot reaction.</p>

<p>O-Benzyl psilocybin is a hydrophobic molecule with an affinity for lipase. It has been shown to exhibit growth inhibition on malignant cells in tissue culture, and has been investigated as a potential anticancer agent. O-Benzyl psilocybin is also able to inhibit the activity of plasminogen activator inhibitor-1 (PAI-1), which is involved in cancer progression and metastasis. This compound may be used as an anticancer drug or as a prophylactic agent against cancer. It may also be useful in treating other conditions such as atherosclerosis and restenosis, where PAI-1 plays a significant role. O-Benzyl psilocybin has been found to have anti-inflammatory properties that may be due to its ability to inhibit the production of prostaglandin E2 from arachidonic acid.</p>

<p>Please enquire for more information about (3-IMidazol-1-yl-propyl)-[4-(4,4,5,5-tetraMethyl-[1,3,2]dioxaborolan-2-yl)-benzyl]aMine including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Bis(trimethylsilyl)acetylene (bis-TMS) is a reactive ancillary that can be used in polymerization reactions as an initiator. The bis-TMS is prepared by reaction of trimethylsilyl chloride with acetylene to form the trimethylsilyl acetylene, which is then reacted with copper to generate the bis-TMS. Bis-TMS reacts with nucleophiles such as alcohols and amines to produce polymers through a nucleophilic attack. It also has been used for sample preparation for NMR spectra. Bis-TMS is a synthetic compound that has been characterized using nmr spectroscopy and analytical methods. The molecular formula of bis-TMS is C8H16Si2 and its molecular weight is 196.13 g/mol. The chemical structure of bis-TMS consists of two benzyl groups connected by a single carbon bond at the 3 o'clock position on the central</p>

<p>Epsilon-Carotene is a carotenoid that is found in plants. It is synthesized from beta-carotene through the action of enzymes called beta-carotene ketolases. Epsilon-Carotene can be cleaved by enzymes to produce lycopene and beta-cryptoxanthin. The biosynthesis of Epsilon-Carotene has been studied in a number of clinical studies, including the effect on human tissues and the prevention of cancer. Epsilon-Carotene has also been shown to have anti-inflammatory properties, which may be due to its ability to inhibit prostaglandin synthesis.</p>

<p>Please enquire for more information about (3-Chloropropyl)diphenylsulfonium tetrafluoroborate including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Diethylsilane is a chemical species that has a high value. It is an inorganic compound that contains silicon and boron, which are both chemical elements. Diethylsilane has been shown to react with hydroxy groups on the surface of many different materials, such as aluminum oxide or steel. The reaction between diethylsilane and the hydroxyl group results in the formation of silicon-hydrogen bonds, which are strong and stable. This reaction mechanism can be used for synthesizing solids with high values, such as boron nitride.</p>

<p>cis-1-Propene-1-boronicacid is a chiral, pyranoside compound that can be synthesized from the reaction of 2,3,4,5-tetrahydropyran with boron trichloride. cis-1-Propene-1-boronicacid has been shown to be useful for the palladium catalyzed cross coupling reactions. cis-1-Propene-1-boronicacid has been shown to react with cyclopentenone and alkylate different functional groups such as amines and alcohols. cis-1 -Propene 1 boronic acid has been used in peptidomimetics as well as in nature.</p>

<p>Trimethylsilyl isocyanate (TMISC) is a 5-membered heteroaryl. It has been shown to bind to the receptor and shows activity in vitro. TMISC has been reported as a potential drug for bowel disease, congestive heart, and inflammatory bowel disease. TMISC binds to the protein receptor with high affinity, but its binding affinity decreases when it is combined with trifluoroacetic acid or palladium-catalyzed coupling. TMISC can be used to synthesize degarelix acetate, which is an anti-androgen drug that is used in the treatment of prostate cancer.</p>

<p>2-(4-(4,4,5,5-Tetramethyl-l,3,2-dioxaborolan-2-yl)phenyl)ethanol is a fine chemical that has been used as a reagent and as a building block for the synthesis of complex compounds. It is also an intermediate in organic reactions and has been used as a reaction component in the synthesis of various drugs and agrochemicals. 2-(4-(4,4,5,5-Tetramethyl-l,3,2-dioxaborolan-2-yl)phenyl)ethanol is useful as a scaffold in organic synthesis. This compound can be converted to other useful chemicals such as tetrahydropyranones and dibenzalacetone derivatives. 2-(4-(4,4,5,5-Tetramethyl-l,3,2-dioxaborolan-2-yl)phenyl)ethanol</p>

<p>Please enquire for more information about 4-(N-Methylamino)phenylboronic acid pinacol ester including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>m-Carborane is a molecule that is composed of a chlorine atom and an aromatic hydrocarbon. m-Carborane has been shown to be an estrogen receptor modulator, which may have potential as a drug for the prevention or treatment of hormone-related diseases. This compound has also been shown to act as a fluorophore and to have high melting points. It forms hydrogen bonds with other molecules and can bind to progesterone receptors, which are found in breast cancer cells. These interactions have been studied using x-ray crystal structures and microscopy studies on MCF-7 cells.</p>

<p>Trichlorooctadecylsilane is a model system that consists of a monolayer of octadecyltrichlorosilane particles. The dispersive solid-phase extraction technique can be used to extract analytes from the surface of this particle. This technique involves removing the solvent from a sample by passing it through an adsorbent. The hydrophobic effect, which is the phenomenon that a nonpolar substance is dissolved in a nonpolar solvent, will cause analytes to bind to the hydrophobic surface of octadecyltrichlorosilane particles because they are hydrophobic.</p>

<p>p-Carborane is a compound that has been used in the palladium-catalyzed coupling of nitrogen atoms. It has been shown to have magnetic resonance spectroscopy, steric interactions, and cross-coupling properties. p-Carborane is stable under mild conditions and can be used as an alternative to other functional assays. p-Carborane also has been shown to inhibit the growth of prostate cancer cells and human leukemia cells (HL60). The redox potentials for this compound are low energy, making it difficult for these compounds to react with other substances.</p>

<p>Dimethoxymethylphenylsilane is a chemical compound that can be used as a substrate film. It is commonly used in gravimetric analysis, thermal expansion, and electrochemical impedance spectroscopy. Dimethoxymethylphenylsilane has been shown to form cationic polymers when heated with fatty acids. This polymerization process requires hydrochloric acid for activation. Dimethoxymethylphenylsilane has also been shown to react with zirconium oxide at high temperatures and form a reactive surface layer of titanium dioxide on the surface of the zirconium oxide. The molecule consists of an oxygen atom, two methyl groups, and two phenyl groups. The solid catalyst has a diameter of approximately 1 nm and its NMR spectra are consistent with those expected for this type of molecule.</p>

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

<p>Dichlorodiisopropylsilane is a cycloaddition process, which is the addition of two molecules to create a new ring. It reacts with an unsaturated organic compound, such as an alkene or alkyne, to produce a reactive functional group. Dichlorodiisopropylsilane has been used in chemistry as a cross-linking agent for proteins and as a solid catalyst. The chemical stability of dichlorodiisopropylsilane makes it useful in the synthesis of model proteins. This compound also has low bioavailability due to its high reactivity with hydrochloric acid found in the stomach.</p>

<p>Please enquire for more information about 5-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)isoindolin-1-one 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 N,N-Dimethyl 4-boronobenzenesulfonamide 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 9,9-Bis(2-ethylhexyl)fluorene-2,7-bis(boronic acidpinacolester) including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>1-Bromomethyl-o-carborane is a boron compound that has been used as a cross-coupling reagent for the conversion of terminal alkynes to acetonitrile. This reagent is prepared by the reaction of lithium diisopropylamide with dicarbonyl compounds, followed by desilylation and alkylation. The hydroxy group can be substituted with triflates or monosubstituted groups. The nature of these substituents will depend on the desired product and reaction conditions. 1-Bromomethyl-o-carborane has been shown to form hyaluronic acid in yields of up to 98%.</p>

<p>Triisopropanolamine borate is an organic compound with the formula (CH3)3N(CH2)3OH. It is a colorless liquid with a sweet, amine-like odor. Triisopropanolamine borate is widely used as a cross-linking agent in coatings, and as a reactive functional group in polycarboxylic acid synthesis and cationic polymerization. It also has been used as a blood pressure lowering agent and to treat high calcium levels in the blood. The chemical structure of triisopropanolamine borate can be seen below: Triisopropanolamine Borate, Chemical Structure The chemical formula for triisopropanolamine borate is CH3N(CH2)3OH. Triisopropanolamine borate has many applications due to its reactive functional groups, including cross-linking agents for coatings and polycarboxylic acid synthesis</p>

<p>Please enquire for more information about 3-Chloro-4-methoxyphenylboronic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>2-Chloro-3-ethylbenzoxazolium tetrafluoroborate is a synthetic compound that inhibits the enzyme maltase. This compound is used in the treatment of diabetic patients with intestinal maltase deficiency and has been shown to be effective in clinical studies. 2-Chloro-3-ethylbenzoxazolium tetrafluoroborate has also been shown to inhibit other enzymes, such as thiocarbamate synthetase and aminooxazoline synthetase, which are involved in the biosynthesis of chlorinated pesticides and herbicides. The chloride ion is necessary for this inhibition activity. The compound can be prepared by a preparative method that involves hexaacetate and chloride ion or by using an aglycone, trehalamine, or stereospecific method.</p>

<p>(+)-B-Chlorodiisopinocampheylborane is a chiral organoboron reagent that can be used for the enantioselective synthesis of amines. It is prepared from the reaction of chlorodiphenyl borane with (+)-diaminobenzene in hexane. The product can be purified by column chromatography or recrystallization. (+)-B-Chlorodiisopinocampheylborane can also be used in the synthesis of other compounds, such as pyrroles and pantolactones. It is an excellent catalyst for the dehydration of primary amines to give unsymmetrical ketones. This reagent has been shown to be effective in asymmetric hydrogenation reactions, such as the reduction of chiral secondary alcohols, and is also capable of catalyzing aldol reactions.</p>

<p>Please enquire for more information about 3-(4-Oxopiperidine-1-carbonyl)phenylboronic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>N-(2-Aminoethyl)-3-aminopropylmethyldimethoxysilane is an antibacterial agent that inhibits the growth of bacteria by binding to the cell wall, thereby preventing the synthesis of proteins. It is used in dentistry and medicine as a coating for metal surfaces. This compound has been shown to be effective against Escherichia coli and Enterococcus faecalis. The optimum concentration for this compound is 1 mg/mL.</p>

<p>Please enquire for more information about 5-Fluoropyridine-2-boronic acid 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 [2-(Difluoromethyl)phenyl]boronic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Ethylanine-boron trifluoride complex (EBTF) is a reactive intermediate that is used in the synthesis of epoxy resins. EBTF reacts with dibutyltin oxide to produce a boron-containing reaction product. The mechanism of this reaction has been studied using fluorescence probes and is found to be dependent on temperature and concentration. EBTF also reacts with epoxides, glycol ethers, and fatty acids to form similar products with different structures. This chemical can be used as a thermal expansion agent for coatings or as a crosslinking agent in polymers.</p>

<p>The trimethylsilyloxy group is a very efficient method for the synthesis of antireflection coatings consisting of metal carbonyls. One such metal carbonyl is tetradentate zirconium oxide. Tetradentate zirconium oxide has been shown to be a good catalyst for the reaction between triflic acid and 1-(trimethylsilyloxy)cyclohexene. The ethyl group on the 1-carbon atom of 1-(trimethylsilyloxy)cyclohexene allows it to coordinate with the zirconium atom in tetradentate zirconium oxide, while the triflic acid acts as an acid catalyst to increase the rate of reaction.</p>

<p>4-(Ethoxycarbonyl)phenylboronic acid is a potential use for picric acid detection. It has been shown to be a chemosensor with an electrochemical impedance spectroscopy response that is sensitive to chloride ions. 4-(Ethoxycarbonyl)phenylboronic acid can be used as a linker in multigram-scale synthesis of aryl halides, and its reaction mechanism has been elucidated by crystal x-ray diffraction. The synthesis of this compound is scalable and involves the formation of an apical carboxylate from ethoxycarbonyl phenyl boronic acid and an aryl halide.</p>

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

<p>(4-Aminophenyl)boronic acid pinacol ester is a semiconducting material that can be used in thin film devices. It has been shown to be a good candidate for transistor and device applications due to its high yield, low cost, and high stability. This compound can also be used to modify the structure of other compounds through substitution reactions. (4-Aminophenyl)boronic acid pinacol ester has been synthesized from inexpensive starting materials, such as triphenylamine and amines.</p>

<p>4-Isopropoxyphenylboronic acid is a boronic acid that can be used as a cross-coupling partner in palladium-catalyzed cross-coupling reactions. It is synthesized by reacting 4-hydroxyphenylacetic acid with 2 equivalents of naphthoquinone diazide. The addition of the 4-isopropoxy group to the phenyl substituent increases the reactivity of this boronic acid. This compound has been used in the synthesis of rofecoxib and cyclooxygenase inhibitors, such as aspirin and ibuprofen. The presence of an electron withdrawing group on one phenyl ring enhances the reactivity of this boronic acid towards nucleophiles, such as amines or alcohols.</p>

<p>2-Aminopyrimidine-5-boronic acid pinacol ester is a boronic acid derivative that has been shown to inhibit the activity of protein kinase C. This compound is also an effective linker for cross-coupling reactions and has a low reactivity with nucleophiles, which makes it safer than other boronic acids. 2-Aminopyrimidine-5-boronic acid pinacol ester has been shown to be potent against cancer cells in vitro and in vivo and synthetic cells. 2-Aminopyrimidine-5-boronic acid pinacol ester inhibits the growth of cancer cells by binding to the ATP site on protein kinase C, thereby inhibiting its function.</p>

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

<p>N-Hexylboronic acid is an organometallic compound that has been used as a model system to study the catalytic mechanism of the Suzuki coupling reaction. It has also been shown to be a substrate film for use in the suzuki coupling reaction when combined with Raney nickel, which can be used to synthesize organic compounds. N-Hexylboronic acid has been shown to inhibit the activity of pancreatic lipase, but not cholesterol esterase or cholesterol ester hydrolase. The skeleton of this molecule is made up of six carbon atoms and one boron atom. Hydrogen chloride and aliphatic hydrocarbons are inhibitors of N-hexylboronic acid.</p>

<p>(-)-B-Chlorodiisopinocampheylborane is a carbonyl group that can be used for asymmetric synthesis. It was synthesized from the reaction of chlorodiisopinocampheylborane with butyllithium and allyl bromide, followed by aqueous workup. The enantiomers were separated through thin layer chromatography on silica gel plates with hexane as the eluent. The resolution of racemic latanoprost lactol was achieved in the same manner. (-)-B-Chlorodiisopinocampheylborane is also a diketone that can be prepared from para-chloroacetophenone and sodium hydroxide in ethanol. This diketone undergoes an intramolecular cyclization to produce noradrenaline (norepinephrine) and hydrochloric acid, which can then be converted into dioxolanes or other products.</p>

<p>Tetrahydroxydiborane is an organic compound that contains a hydroxyl group. It has been shown to be an effective nucleophile in the mechanism studies of hydrolysis of halides and nitro compounds. Tetrahydroxydiborane is also used in the Suzuki coupling reaction, which is a chemical reaction between an aryl halide and sodium carbonate, as well as in cationic polymerization. This compound may also have biological applications such as the use of tetrahydroxydiborane as a fluorescence probe for optical sensor detection of autoimmune diseases.</p>

<p>Lithium difluoro(oxalato)borate is an electron-microscopic corrosion inhibitor that belongs to the class of ester compounds. It is a solid compound that has been shown to be efficacious against oxidation products. The efficiency of this compound is dependent on the concentration and purity of lithium difluoro(oxalato)borate and the type of metal, such as steel or aluminum. Lithium difluoro(oxalato)borate can be used in rechargeable batteries, due to its transport properties, high salt tolerance, and low self-discharge rate. This compound has been shown to have functional groups that are capable of interacting with hydrogen fluoride in an organic solution.</p>

<p>Triisopropylsilylacetylene is an aliphatic hydrocarbon with a reactive site that can be used in the synthesis of other chemical compounds. It has been shown to have an inhibitory effect on the formation of reactive oxygen species and inflammation in mice, which may be due to its ability to reduce the production of inflammatory mediators such as prostaglandin E2. Triisopropylsilylacetylene also has a hydroxyl group, which allows it to act as an anti-inflammatory agent by inhibiting the enzyme cyclooxygenase. Additionally, triisopropylsilylacetylene has a carbonyl group, which gives it aromatic properties that can be used for synthetic purposes.</p>

<p>Epsilon caprolactam is a poly-functional compound that can be used as a monomer for the production of polyamides. It is produced from lysine and caproic acid in the presence of copper chloride by oxidative decarboxylation. Epsilon caprolactam has been shown to have synergistic effects with other compounds, such as toxicity studies on rats and mice. This compound also has an acidic nature due to its carboxylic acid group. Plasma mass spectrometry has shown that there are high values of epsilon caprolactam in the plasma of bacterial strains and it is rapidly metabolized to l-lysine. Epsilon caprolactam is also a solid catalyst for organic reactions, which causes phase transition temperature to increase and promotes reaction mechanisms.</p>

<p>Silyl protecting group for alcohols; reagent for introducing protected C atom</p>

<p>Please enquire for more information about 1-Methylindole-3-boronic acid pinacol ester including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Vinyloxytrimethylsilane is an organosilicon compound that is used as a polymerization initiator. It reacts with cyclobutanone to form a ruthenium complex, which can be used to coat surfaces and produce polymers. The use of this compound has been shown to increase the reaction yield and decrease the amount of by-products in the polymerization process. Vinyloxytrimethylsilane is biodegradable, making it an environmentally friendly alternative for coating surfaces or producing polymers.</p>