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.
3,5-Dichloro-2-hydroxybenzenesulfonyl chloride is used in the synthesis of (1R,2R)-(+)-1,2-(3,3?,5,5?-tetrachloro-2,2?-dihydroxydibenzenesulfonamido)-1,2-diphenylethane1 and (1R,2R)-(+)- 1,2-(3,3?,5,5?-tetrachloro-2,2?-dihydroxydibenzenesulfonamido)cyclohexane. It was used as chromogenic system in one-step kinetic method for the determination of 5?-nucleotidase.
A Bertrand; J Buret. A one-step determination of serum 5'-nucleotidase using a centrifugal analyzer. Clinica Chimica Acta.1982, 119, (3), 275-284.
Cheng Guo; Jun Qiu; Xumu Zhang; Dawn Verdugo; Martin L. Larter; Ray Christie; Patrick Kenney; Patrick J. Walsh. Enantioselective addition of diethylzinc to benzaldehyde catalyzed by chiral titanate complexes with helical ligands. Tetrahedron.1997, 53, 4145-4158.
Reagent for peptide coupling with low racemization: Tetrahedron Lett., 35, 9561 (1994). See Appendix 6. Reaction is thought to proceed via an o-thioquinone S,S-dioxide, leading to a carboxylic sulfonic mixed anhydride which rearranges to an active ester:
Gefahrenhinweise (EU): H314-H318
Causes severe skin burns and eye damage. Causes serious eye damage.
Do not breathe dusts or mists. 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.