![[2,5-dimethyl-1-(4-methylphenyl)-1H-pyrrol-3-yl]-N,N,N-trimethylmethanaminium iodide (CAS 1025737-67-0) - chemical structure](https://media.scbt.com/product/2-5-dimethyl-1-4-methylphenyl-1h-pyrrol-3-yl-n-n-n-trimethylmethanaminium-iodide-structure_25_18_b_251895.jpg)
![[2,5-dimethyl-1-(4-methylphenyl)-1H-pyrrol-3-yl]-N,N,N-trimethylmethanaminium iodide (CAS 1025737-67-0) - chemical structure](https://media.scbt.com/product/2-5-dimethyl-1-4-methylphenyl-1h-pyrrol-3-yl-n-n-n-trimethylmethanaminium-iodide-structure_25_18_t_251895.jpg "Molecular structure of [2,5-dimethyl-1-(4-methylphenyl)-1H-pyrrol-3-yl]-N,N,N-trimethylmethanaminium iodide, CAS Number: 1025737-67-0")
[2,5-dimethyl-1-(4-methylphenyl)-1H-pyrrol-3-yl]-N,N,N-trimethylmethanaminium iodide (CAS 1025737-67-0)
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[2,5-dimethyl-1-(4-methylphenyl)-1H-pyrrol-3-yl]-N,N,N-trimethylmethanaminium iodide also known as {[2,5-dimethyl-1-(4-methylphenyl)-1H-pyrrol-3-yl]methyl}trimethylazanium iodide, is a widely used quaternary ammonium salt in scientific research. Its unique properties make it an excellent reagent for diverse chemical reactions. 2,5-dimethyl-1-(4-methylphenyl)-1H-pyrrol-3-yl]-N,N,N-trimethylmethanaminium iodide finds application as a reagent in the synthesis of quaternary ammonium salts, alkylating amines, and producing heterocyclic compounds. It also acts as a catalyst in various reactions, including the synthesis of cyclic carbonates from epoxides and carbon dioxide. It is functions as a nucleophile, attacking electrophilic species and forming quaternary ammonium salts.
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
[2,5-dimethyl-1-(4-methylphenyl)-1H-pyrrol-3-yl]-N,N,N-trimethylmethanaminium iodide, 250 mg | sc-343488 | 250 mg | $192.00 | |||
[2,5-dimethyl-1-(4-methylphenyl)-1H-pyrrol-3-yl]-N,N,N-trimethylmethanaminium iodide, 1 g | sc-343488A | 1 g | $388.00 |