Molecular structure of S-Methyl N-(2,2,2-trichloroethoxysulfonyl)carbonchloroimidothioate
S-Methyl N-(2,2,2-trichloroethoxysulfonyl)carbonchloroimidothioate
Molecular Weight:
321.03
Molecular Formula:
C4H5Cl4NO3S2
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.
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A reagent used for the preparation of protected guanidine derivatives.
S-Methyl N-(2,2,2-trichloroethoxysulfonyl)carbonchloroimidothioate References
- Expanding the substrate scope for C-H amination reactions: oxidative cyclization of urea and guanidine derivatives. | Kim, M., et al. 2006. Org Lett. 8: 1073-6. PMID: 16524271
- Total synthesis of (-)-muraymycin D2 and its epimer. | Tanino, T., et al. 2010. J Org Chem. 75: 1366-77. PMID: 20143822
- Total synthesis of (+)-cylindradine A. | Iwata, M., et al. 2014. Chem Commun (Camb). 50: 6991-4. PMID: 24846327
- The chemistry and biology of guanidine natural products. | Berlinck, RG. and Romminger, S. 2016. Nat Prod Rep. 33: 456-90. PMID: 26689539
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| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
S-Methyl N-(2,2,2-trichloroethoxysulfonyl)carbonchloroimidothioate, 5 g | sc-301717 | 5 g | $330.00 |