Related Experiment Video
Updated: Aug 22, 2025

Preparation of N-2-alkoxyvinylsulfonamides from N-tosyl-1,2,3-triazoles and Subsequent Conversion to Substituted Phthalans and Phenethylamines
Published on: January 3, 2018
2-(Octa-decyl-sulfan-yl)-1,3-thia-zole
Joseph E Muller Ii1, Laura R Osborn2, Joseph R Traver2
1Department of Chemistry and Physics, Florida Gulf Coast University, 10501 FGCU Blvd. South, Fort Myers, FL, 33965, USA.
Abstract:
The title compound, C21H39NS2, crystallizes with two mol-ecules in the asymmetric unit, both having a linear 18-carbon alkyl chain bound through a thio-ether group. No π-π stacking or hydrogen bonding is observed. The orientation of the alkyl chains facilitates inter-molecular inter-actions between te chains. The structure is metrically ortho-rhom-bic but crystallizes in the monoclinic space group P21 and was found to be twinned by pseudomerohedry (emulating ortho-rhom-bic symmetry) and by inversion. The twin factions refined to 0.37 (4), 0.13 (4), 0.31 (5), and 0.19 (4).
More Related Videos
08:51Scale-up Chemical Synthesis of Thermally-activated Delayed Fluorescence Emitters Based on the Dibenzothiophene-S,S-Dioxide Core
Published on: October 24, 2017
08:47Synthesis and Bioconjugation of Thiol-Reactive Reagents for the Creation of Site-Selectively Modified Immunoconjugates
Published on: March 6, 2019
Related Concept Videos
Preparation and Reactions of Thiols
Structure and Nomenclature of Thiols and Sulfides
Preparation and Reactions of Sulfides