Trimethylsilyl isothiocyanate (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "Trimethylsilyl isothiocyanate" in English language version.

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alfa.com

"Trimethylsilyl isothiocyanate, 94%". Alfa Aesar. Thermo Fisher Scientific. Retrieved April 9, 2020.
"Safety Data Sheet". Alfa. Thermo Fisher Scientific. Retrieved April 10, 2020.

Guda, Dinneswara Reddy; Wang, Tengjiao; Cho, Hyeon Mo; Lee, Myong Euy (September 2012). "Trimethylsilyl isothiocyanate (TMSNCS): an efficient reagent for the one-pot synthesis of mercapto-1,2,4-triazoles". Tetrahedron Letters. 53 (39): 5238. doi:10.1016/j.tetlet.2012.07.054.
Renard, Pierre-Yves; Schwebel, Hervé; Vayron, Philippe; Leclerc, Eric; Dias, Sonia; Mioskowski, Charles (2001). "Optimized access to alkyl thiocyanates". Tetrahedron Lett. 42 (48): 8479–8481. doi:10.1016/S0040-4039(01)01846-9.
Nishiyama, Kozaburo; Oba, Makoto (June 1987). "Reactions of Trimethylsilyl Isothiocyanate with Aldehydes and Acetals. Synthesis of Symmetrically and Unsymmetrically Isothiocyanato-Substituted Ethers". Bulletin of the Chemical Society of Japan. 60 (6): 2289–2291. doi:10.1246/bcsj.60.2289.
Guda, Dinneswara Reddy; Cho, Hyeon Mo; Lee, Myong Euy (2013). "Mild and convenient one-pot synthesis of 2-amino-1,3,4-oxadiazoles promoted by trimethylsilyl isothiocyanate (TMSNCS)". RSC Advances. 3 (21): 7684. Bibcode:2013RSCAd...3.7684G. doi:10.1039/C3RA41044G. Retrieved 10 April 2020.

"Trimethylsilyl isothiocyanate". Summary of Classification and Labeling. European Chemicals Agency (ECHA). Retrieved April 9, 2020.

Guda, Dinneswara Reddy; Cho, Hyeon Mo; Lee, Myong Euy (2013). "Electronic Supplementary Information (ESI)" (PDF). The Royal Society of Chemistry: S1–S8. Retrieved 10 April 2020.