N-Boc-5-bromoindole
N-Boc-5-bromoindole can undergo Sonogashira coupling reaction with N,N-diisopropylprop-2-ynylamine to afford the corresponding propargylic diisopropylamine. N-Boc-5-bromoindole is formed as an intermediate during the synthesis of 2-(5-substituted-1H-indol-3-yl)-N-hydroxyacetamide derivatives.
| Catalog Number | CBB1133487 |
| Alternative Name(s) | tert-Butyl 5-bromoindole-1-carboxylate |
| Molecular Formula | C13H14BrNO2 |
| CAS# | 182344-70-3 |
| Purity | >97% |
| Inchi | 1S/C13H14BrNO2/c1-13(2,3)17-12(16)15-7-6-9-8-10(14)4-5-11(9)15/h4-8H,1-3H3 |
| Inchi Key | PBWDRTGTQIXVBR-UHFFFAOYSA-N |
| SMILES | CC(C)(C)OC(=O)n1ccc2cc(Br)ccc12 |
| Size | Inquiry |
| Supplier Page | https://www.amerigoscientific.com/n-boc-5-bromoindole-item-133487.html |