Organoboranes

<p>Applications Trimethylsilyl azide is used to mediate Schmidt rearragement reactions and is also used as a nucleophile in organic synthesis. Versatile azidonation reagent for amines, amides, aldehydes, and ketones.<br> Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package<br>References Mphahlele, M.: J. Chem. Soc. Perk. T. 1, 23, 3477 (1999); Pastor, I. &amp; Yus, M.: Org. Chem., 9, 1 (2005)<br></p>

<p>Applications Hydrogen Tetrafluoroborate(1-) is a useful building block for organic synthesis.<br>References Ohkuma, T., et al.: Journal of the American Chemical Society., 218, 8724 (2006)<br></p>

<p>Applications Used to protect alcohols during organic synthesis.<br>References Shen, H., et al.: J. Med. Chem., 53, 2666 (2010), Qiang, L., et al.: Bioorg. Med. Chem. Lett., 20, 836 (2010),<br></p>

<p>Applications OCTADECYLTRIETHOXYSILANE (cas# 7399-00-0) is a useful research chemical.<br></p>

<p>Applications N,O-Bis(trimethylsilyl)acetamide is used as a reagent in the synthesis of 4'-spirocyclic phosphono-nucleosides as potential inhibitors of hepatitis C virus NS5B polymerase. Also used as a reagent in the microwave-assisted synthesis of purine nucleosides as selective cholinesterase inhibitors.<br> Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package<br>References Dang, Q., et al.: Tetrahedron Lett., 55, 4407 (2014); Schwarz, S., et al.: Org. Biomol. Chem., 12, 2446 (2014)<br></p>

<p>Applications Hydroxydi-p-tolylborane is a building block used as a reactant in the nickel-catalyzed cross-coupling of diarylborinic acids with aryl chlorides.<br>References Chen, X., et al.: ACS Catalys., 4, 379 (2014);<br></p>

<p>Stability Light and Temperature sensitive<br>Applications PFPA-silane is a functionalized perfluorophenyl azides for covalent immobilization of ultrathin polymer films.<br>References Mosbach, K., et al.: Biotechnology, 14, 163 (1996), Keren, K., et al.: Science, 297, 72 (2002), Lidstrom, M., et al.: Nature Rev. Microbiol., 1, 158 (2003),<br></p>

<p>Applications (E)-2-(1-Butenyl)-1,3,2-benzodioxaborole (cas# 106094-36-4) is a compound useful in organic synthesis.<br></p>

<p>Applications Tetramethylammonium Triacetoxyborohydride is used in the synthesis of Peloruside A. Epoxypropanoate is a neurokinin substance P receptor antagonist synthesized from this compound.<br> Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package<br>References Gazaille, J. et al.: Org. Lett., 14, 178 (2012); Prevost, S. et al.: Tetrahedron Asymm., 21, 16 (2010);<br></p>

<p>Applications 2-Fluoro-3-methoxyphenylboronic acid<br></p>

<p>Applications Heptamethylcyclotetrasiloxan-2-ol is a derivative of Octamethylcyclotetrasiloxane (O237145), which is an organometallic reagent that can be used in the preparation of siloxane polymers, with high surface-hydrophobicity restoration.<br>References Fritz, O., et al.: MRS Online Proceedings Library, 1535 (2012); Vanossi, A., et al.: Condensed Matter (2013);<br></p>

<p>Stability Moisture Sensitive<br>Applications Chlorotrimethylsilane have been used in the preparation of volatile derivatives of a wide range of compounds for GC analysis. Chlorotrimethylsilane has been used for silylation and as a protection group in the process of various organic synthesis.<br> E0<br>References Casimiro, M., et al.: Org. Lett., 15, 2378 (2013); Lifchits, O., et al.: J. Am. Chem. Soc., 135, 6677 (2013);<br></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>(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-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>N-alpha-Boc-Nepsilon-Z-D-lysine is a fusogenic peptide that has an acidic pKa. It is a potent inhibitor of survivin, which is a protein that regulates cell death. It also inhibits the uptake of l-phenylalanine to promote cancer cell death. The functional groups on this compound are epoxyketones, which have regulatory properties as well as being able to inhibit the growth of cells.</p>

<p>Tris(trimethylsilyl)silane is a reactive functional group that is used in the synthesis of monoclonal antibodies. It reacts with halides to form an intermediate, which then undergoes chain reactions with other molecules to form the final product. Tris(trimethylsilyl)silane can be used for cancer therapy and for the detection of antibodies. It has been shown that tris(trimethylsilyl)silane will react with a light emitting compound (e.g., 4-dimethylaminopyridine) and a cationic polymerization initiator (e.g., diallyldimethylammonium chloride). This reaction produces high values of light emission, which can be detected by x-ray crystal structures.</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>Nepsilon-4-nitro-Z-L-lysine is a plant nutrient that can be used in agricultural and horticultural applications. It is a particle that can be added to the soil to improve fertility and stimulate plant growth. Nepsilon-4-nitro-Z-L-lysine has been shown to have a protective effect on plants against insect pests and fungal infections, as well as inhibiting the formation of toxic compounds during fermentation. This product also provides an alternative to chemical treatment and can be used for environmental monitoring or mesoscale studies. Nepsilon-4-nitro-Z-L-lysine has been shown to improve horse fertility and reduce the number of treatments required for resistant bacterial infections.</p>

<p>Lithium tetraborate (LiBO) is a compound used in the preparation of samples for laser ablation. It can be synthesized by reacting lithium carbonate with boron nitride in a hydrochloric acid solution at room temperature. Lithium tetraborate is often used as a buffer to increase the pH of the solution and to maintain it at a constant level during reactions. This compound has been studied extensively, and its spectroscopic properties have been well documented. The thermal expansion coefficient of LiBO is high, which makes it suitable for use in radiation experiments. Lithium tetraborate has also been shown to be an effective catalyst for organic synthesis reactions that require high activation energies, such as the synthesis of phenol from benzene and formaldehyde.</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>(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>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>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>(R)-(-)-3,3′-Bis(triphenylsilyl)-1,1′-binaphthyl-2,2′-diyl hydrogenphosphate is a fine chemical that is a useful reagent and building block. It can be used as an intermediate in the synthesis of complex compounds. This chemical has a CAS number of 791616-55-2 and is classified as a speciality chemical. (R)-(-)-3,3′-Bis(triphenylsilyl)-1,1′-binaphthyl-2,2′-diyl hydrogenphosphate is also a versatile building block for the synthesis of reaction components with high quality.</p>

<p>Tert-butyldimethylsilyl chloride is a silicon-containing compound that is used to prepare the tert-butyl group, which is an important part of many organic compounds. Tert-butyldimethylsilyl chloride reacts with trifluoroacetic acid to form hydrogen bonds. It can also react with hydrochloric acid to form a tert-butyl chloride, which is soluble in water and hydrolyzes in human serum. Tert-butyldimethylsilyl chloride has been used for the synthesis of carbohydrates and fatty acids. It has been used as a sample preparation agent for gas chromatography mass spectrometry and high performance liquid chromatography. The reaction solution can be prepared by reacting tert-butyldimethylsilyl chloride with an alcohol or carboxylic acid in the presence of base at low temperature. Tert-butyldimethylsilyl chloride can be synthesized by reacting</p>

<p>5-Formyl-2-thiopheneboronic acid is a synthetic molecule that has been shown to be an effective electron microscope stabilizer. It is a boronate ester with a formyl group at the 2-position and a thiophene ring at the 5-position. The chloride in this molecule is used as a functional group, which can then react with other molecules to form new compounds. The functional theory of 5-formyl-2-thiopheneboronic acid includes its ability to form bonds with other molecules and its use as an inorganic base. The particle size of 5-formyl-2-thiopheneboronic acid is unsymmetrical, making it different from other molecules.</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>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>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>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>4,4,5,5-Tetramethyl-2-(1,4-dioxaspiro[4.5]dec-7-en-8-yl)-1,3,2-dioxaborolane is a pinacol ester that can be polymerized to form polytetrafluoroethylene (PTFE). It has a high reactivity and is used as a monomer in the production of PTFE.</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-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>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>(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>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>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>N,N'-4,4'-Bis(benzyl-2-boronic acid)-bipyridinium dibromide is a high quality reagent that can be used as an intermediate for the synthesis of complex organic compounds. It is a complex compound that contains boronic acid and bipyridinium moieties. N,N'-4,4'-Bis(benzyl-2-boronic acid)-bipyridinium dibromide is useful in the synthesis of fine chemicals and speciality chemicals. It has versatile building block properties and can be used as a reaction component in many chemical reactions.</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>(3R,4R)-4-Acetoxy-3-[(R)-1-(tert-butyldimethylsilyloxy)ethyl]-2-azetidinone is a versatile building block that can be used as a reagent and speciality chemical. It is also a useful scaffold for the synthesis of complex compounds. It has been shown to be useful in the manufacture of research chemicals and other fine chemicals. This compound is characterized by its high quality and can be used as an intermediate in reactions involving nucleophilic substitution, alkylation, acylation, esterification, and amination.</p>