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1-Chloro-3-iodopropane undergoes asymmetric alpha-alkylation with N-sulfinyl imidates to yield 2-substituted N-tert-butanesulfinyl-5-chloropentanimidates. Electroreduction of 1-chloro-3-iodopropane at glassy carbon electrode in dimethylformamide containing tetra-n-butylammonium perchlorate has been investigated by cyclic voltammetry. It also participates in conjugate addition of alkyl iodides to alpha,beta-unsaturated nitriles in water.
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
1-Chloro-3-iodopropane, 25 g | sc-251497 | 25 g | $47.00 |