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The Rosenmund–von Braun synthesis is an organic reaction in which an aryl halide reacts with cuprous cyanide to yield an aryl nitrile. [1] [2] [3]The reaction was named after Karl Wilhelm Rosenmund who together with his Ph.D. student Erich Struck discovered in 1914 that aryl halide reacts with alcohol water solution of potassium cyanide and catalytic amounts of cuprous cyanide at 200 °C.
Solutions of calcium cyanide can be prepared by treating calcium hydroxide with hydrogen cyanide. Solid calcium cyanide is produced commercially by heating calcium cyanamide with sodium chloride. The reaction is incomplete. The product is only of 50% purity, other components being sodium cyanide, calcium cyanamide, and carbon. Because of the ...
A calcium spark is the microscopic release of calcium (Ca 2+) from a store known as the sarcoplasmic reticulum (SR), located within muscle cells. [1] This release occurs through an ion channel within the membrane of the SR , known as a ryanodine receptor (RyR) , which opens upon activation. [ 2 ]
Excitation-contraction coupling in myocardium relies on sarcolemma depolarization and subsequent Ca 2+ entry to trigger Ca 2+ release from the sarcoplasmic reticulum. When an action potential depolarizes the cell membrane, voltage-gated Ca 2+ channels (e.g., L-type calcium channels) are activated.
Calcium signaling is the use of calcium ions (Ca 2+) to communicate and drive intracellular processes often as a step in signal transduction. Ca 2+ is important for cellular signalling , for once it enters the cytosol of the cytoplasm it exerts allosteric regulatory effects on many enzymes and proteins .
Among the most toxic cyanides are hydrogen cyanide (HCN), sodium cyanide (NaCN), potassium cyanide (KCN), and calcium cyanide (Ca(CN) 2). The cyanide anion is an inhibitor of the enzyme cytochrome c oxidase (also known as aa 3), the fourth complex of the electron transport chain found in the inner membrane of the mitochondria of eukaryotic ...
The cyanide source can be potassium cyanide (KCN), sodium cyanide (NaCN) or trimethylsilyl cyanide ((CH 3) 3 SiCN). With aromatic aldehydes such as benzaldehyde, the benzoin condensation is a competing reaction. The reaction is used in carbohydrate chemistry as a chain extension method for example that of D-xylose.
Cyanohydrins are industrially important precursors to carboxylic acids and some amino acids. Cyanohydrins can be formed by the cyanohydrin reaction, which involves treating a ketone or an aldehyde with hydrogen cyanide (HCN) in the presence of excess amounts of sodium cyanide (NaCN) as a catalyst: [1] RR’C=O + HCN → RR’C(OH)CN