p-Toluenesulfonylmethyl isocyanide
p-Toluenesulfonylmethyl isocyanide undergoes base-promoted 1,3-dipolar cycloaddition reaction with immobilized imines under microwave irradiation to yield 1,5-disubstituted imidazoles. It is a versatile synthon in organic chemistry, extensively used for the synthesis of heterocyclic compounds.
Catalog Number | CBB1112145 |
Alternative Name(s) | TosMIC; Tosylmethyl isocyanide; (p-Tolylsulfonyl)methyl isocyanide |
Molecular Formula | CH3C6H4SO2CH2NC |
CAS# | 36635-61-7 |
Purity | >98% |
Inchi | 1S/C9H9NO2S/c1-8-3-5-9(6-4-8)13(11,12)7-10-2/h3-6H,7H2,1H3 |
Inchi Key | CFOAUYCPAUGDFF-UHFFFAOYSA-N |
SMILES | Cc1ccc(cc1)S(=O)(=O)C[N+]#[C-] |
Size | Inquiry |
Supplier Page | https://www.amerigoscientific.com/p-toluenesulfonylmethyl-isocyanide-item-112145.html |