(Trimethylsilyl)isothiocyanate
Trimethylsilyl isothiocyanate (TMS-ITC) reacts with fullerene-mixed peroxide C60(O)(OOtBu)4 to yield isothiocyanate derivative C60(NCS)(OH)(OOtBu)4. TMS-ITC undergoes condensation with ethyl 2-benzylamino-5-methyl-3-phenylcyclopent-1-enecarboxylate to yield 1-benzyl-5-methyl-7-phenyl-2-thioxo-1,2,3,5,6,7-hexahydrocyclopentapyrimidin-4-one. It participates in ring opening reaction of N-substituted aziridines and cyclohexene oxide.
| Catalog Number | CBB1115299 |
| Alternative Name(s) | Isothiocyanatotrimethylsilane |
| Molecular Formula | (CH3)3SiNCS |
| CAS# | 2290-65-5 |
| Purity | >99% |
| Inchi | 1S/C4H9NSSi/c1-7(2,3)5-4-6/h1-3H3 |
| Inchi Key | XLTUPERVRFLGLJ-UHFFFAOYSA-N |
| SMILES | C[Si](C)(C)N=C=S |
| Size | Inquiry |
| Supplier Page | https://www.amerigoscientific.com/trimethylsilylisothiocyanate-item-115299.html |