Organosilicon Compounds

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S20325 - 1-Trimethylsilyl-1,2,4-triazole

Tetrabutylammonium Tetraphenylborate is an enolate anion that is used as a catalyst in organic syntheses. Tetrabutylammonium Tetraphenylborate reacts with aliphatic hydrocarbons to form tertiary alcohols and ketones. Tetrabutylammonium Tetraphenylborate has been shown to produce a viscosity increase of up to 3 times for n-dimethyl formamide. This product also exhibits transport properties, hydrogen bonds, and solubility in human serum. It has been shown to be a model system for polymeric matrices.

3-Bromothiophene-4-boronic acid is an organic compound that is used in chemical synthesis. It reacts with a variety of organic and inorganic compounds to form boronate esters. 3-Bromothiophene-4-boronic acid can be used as the catalyst for many different reactions, including the conversion of aryl chlorides to boronic acids. This compound is also reversibly deprotonated by a nonpolar solvent, such as hexane or chloroform. 3-Bromothiophene-4-boronic acid has been shown to be catalytically active when using an iodide or chloride as an oxidant, which may be due to its high electron density on the heteroatom (i.e., boron).

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Iron(II) tetrafluoroborate is a green-yellow crystalline solid that is soluble in water. It has been shown to have structural and optical properties that are similar to those of ferric chloride, but with the advantage of being less toxic. Iron(II) tetrafluoroborate is used as a homogeneous catalyst for organic reactions such as the hydrogenation of nitroarenes and the reduction of ketones. The catalytic activity of Iron(II) tetrafluoroborate arises from its ability to form hydrogen bonding interactions with other molecules and ions in solution. Iron(II) tetrafluoroborate undergoes a number of reactions with other compounds, including cleavage products such as hydrogen sulfate and nitrogen atoms, which may be due to its chelate ligand. In coordination chemistry, Iron(II) tetrafluoroborate can form coordination complexes by reacting with potassium dichromate or calcium carbonate. These complexes are

(R)-Diphenylprolinol trimethyl silyl ether is a reagent that can be used in organic chemistry. It is prepared by the reaction of diphenylprolinol with trimethylsilyl chloride. The compound can be used as an organocatalyst for the preparation of iminium compounds and carbamates, which are used to synthesize enamines and other compounds. (R)-Diphenylprolinol trimethyl silyl ether is soluble in a variety of solvents, including alcohols, ethers, chlorinated hydrocarbons, and halogenated hydrocarbons. It has been shown to be stable at room temperature and crystalline under ambient conditions.

S20575 - Triphenylfluorosilane

2-Naphthaleneboronic acid pinacol ester (2NBPE) is a boronic acid that can be used as an intermediate in organic synthesis. The compound has been shown to react with different types of molecules, such as flavones, chromanones and biomolecules. 2NBPE is also able to form esters with arylboronic acids, which are then oxidized to yield chromanones. This reaction is catalyzed by oxidative conditions such as hydrogen peroxide or molecular oxygen. 2NBPE can be used for the synthesis of other compounds through the coupling with carbonyls and alcohols.

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2-Formylthiophene-3-boronic acid is a peroxide that is used in cancer research. The compound has been shown to inhibit the growth of pancreatic cancer cells in vitro and in vivo. 2-Formylthiophene-3-boronic acid also inhibits tumor growth and metastasis in animal models of melanoma and breast cancer. In addition, this compound has been shown to be neuroprotective by reducing neuron cell death following ischemia reperfusion. 2-Formylthiophene-3-boronic acid is also an effective inhibitor of DNA synthesis, which may be due to its ability to form conjugates with nucleophiles such as glutathione or thiols on the surface of cancer cells.