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Molar mass: 278.7754 g/mol Appearance white to yellow solid ... Triphenylmethyl chloride or trityl chloride (TrCl) is a white solid with the chemical formula C 19 H ...
Molar mass: 244.337 g·mol −1 ... A trityl group in organic chemistry is a triphenylmethyl group Ph 3 C, e.g. triphenylmethyl chloride ...
Molar mass: 177.94 g·mol −1 ... Triphenylmethyl chloride, also known as trityl chloride. References. a b This page was ...
Triphenylmethanol features three phenyl (Ph) rings and an alcohol group bound to a central tetrahedral carbon atom. All three C–Ph bonds are typical of sp 3-sp 2 carbon-carbon bonds with lengths of approximately 1.47 Å, while the C–O bond length is approximately 1.42 Å.
The triphenylmethyl radical can be prepared by homolysis of triphenylmethyl chloride 1 by a metal like silver or zinc in benzene or diethyl ether. The radical 2 forms a chemical equilibrium with the quinoid-type dimer 3 (Gomberg's dimer). In benzene the concentration of the radical is 2%. [3] Triphenylmethyl radical
It is the thiol derivative of the bulky substituent triphenylmethyl (called trityl). [1] [2] The compound forms a number of unusual derivatives that are more stable than less bulky analogues. The sulfenyl chloride (C 6 H 5) 3 CSCl is obtained from the thiol with sulfuryl chloride. It in turn reacts with ammonia to form the sulfenamide (C 6 H 5 ...
Triphenylphosphine (IUPAC name: triphenylphosphane) is a common organophosphorus compound with the formula P(C 6 H 5) 3 and often abbreviated to P Ph 3 or Ph 3 P. It is versatile compound that is widely used as a reagent in organic synthesis and as a ligand for transition metal complexes, including ones that serve as catalysts in organometallic chemistry.
Molar mass: 228.294 g·mol −1 Appearance white Density: 1.308 g/cm 3 [2] Melting point: 198 °C; 388 °F; 471 K Boiling point: 438 °C; 820 °F; 711 K