I agree Our site saves small pieces of text information (cookies) on your device in order to deliver better content and for statistical purposes. You can disable the usage of cookies by changing the settings of your browser. By browsing our website without changing the browser settings you grant us permission to store that information on your device.
It is considered as a more reactive reagent than Chlorotriphenylmethane, for the preparation of trityl esters. It is also used in one-pot conversion of amino acids to their N-trityl derivatives involving N,O-ditritylation and selective methanolysis of the trityl ester.
Alan C. Scott and John M. Tedder. The induced homolysis of bromotriphenylmethane by a nitroxide.J. Chem. Soc., Chem. Commun.,1979(2), 64b-65.
A. E. Arbuzov and M. Sh. Bastonova. The tautomerism of carbostyril derivatives.Bulletin of the Academy of Sciences of the USSR, Division of chemical science,1952,1(5), 747-754.
More reactive reagent than Chlorotriphenylmethane, A11799 for the preparation of trityl esters: J. Org. Chem., 27, 3595 (1962). One-pot conversion of amino acids to their N-trityl derivatives involves N,O-ditritylation and selective methanolysis of the trityl ester: Synthesis, 198 (1989). See also Appendix 6.
Gefahrenhinweise (EU): H314-H318
Causes severe skin burns and eye damage. Causes serious eye damage.
IF ON SKIN (or hair): Remove/Take off immediately all contaminated clothing. Rinse skin with water/shower. IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continue rinsing. IF SWALLOWED: Rinse mouth. Do NOT induce vomiting. Store locked up. Dispose of contents/container in accordance with local/regional/national/international regulations.