7541-76-6

Usage

Uses

Used in Organic Synthesis:
4-Formyl-N,N,N-trimethylbenzenaminium·iodide serves as a crucial reagent in organic synthesis, where it is employed for the formation of carbon-carbon bonds. Its role in this process is pivotal for creating complex molecular structures that are essential in various chemical and pharmaceutical applications.
Used in Pharmaceutical Compounds:
In the pharmaceutical industry, 4-Formyl-N,N,N-trimethylbenzenaminium·iodide is utilized as a reagent for the modification of organic molecules. This modification is vital for the development of new drugs and the enhancement of existing pharmaceutical compounds, contributing to advancements in medicinal chemistry.
Used in Chemical Research:
4-Formyl-N,N,N-trimethylbenzenaminium·iodide is also applied in chemical research as a tool to explore and understand the reactivity and properties of various organic compounds. Its use in research settings facilitates the discovery of new chemical reactions and the optimization of existing synthetic pathways.

InChI:InChI=1/C10H14NO/c1-11(2,3)10-6-4-9(8-12)5-7-10/h4-8H,1-3H3/q+1

Upstream product

• 100-10-7 4-dimethylamino-benzaldehyde 
• 74-88-4 methyl iodide 
• 79-46-9 2-nitropropane 

Downstream Products

• 3338-65-6 tri-N-methyl-4-(phenylimino-methyl)-anilinium; iodide 
• 1187933-66-9 4-formyl-N,N,N-trimethyl-benzenaminium acetate 
• 28129-11-5 4-formyl-N,N,N-trimethyl-benzenaminium p-toluenesulfonate 
• 1251957-52-4 4-formyl-N,N,N-trimethyl-benzenaminium nitrate 

Relevant academic research and scientific papers

Coacervation of dynamic covalent surfactants with polyacrylamides: Properties and applications

Dynamic covalent surfactants have been prepared from a mixture of 4-formyl-N,N,N-trimethylbenzenaminium iodide (FBA) with heptylamine (C7A) or octylamine (C8A) in alkaline aqueous solutions. The reversible pH-dependent nature of the

Hydrogen Tunneling above Room Temperature Evidenced by Infrared Ion Spectroscopy

While hydrogen tunneling at elevated temperatures has, for instance, often been postulated in biochemical processes, spectroscopic proof is thus far limited to cryogenic conditions, under which thermal reactivity is negligible. We report spectroscopic evi

Preparation of quarternary ammonium salt-tagged ferrocenylphosphine-imine ligands and their application to palladium-catalyzed asymmetric allylic substitution

A series of novel quarternary ammonium salt-modified chiral ferrocenylphosphine-imine ligands have been synthesized and the molecular structure of BIT5 has been determined by single-crystal X-ray diffraction. The applicability of these ligands in asymmetric C*C and C*N bond formation was demonstrated. High enantioselectivity was obtained in the Pd-catalyzed asymmetric substitution of 1,3-diphenyl- 2-propenyl acetate, with dimethyl malonate (up to 94.6% ee) and benzylamine (up to 92.6% ee).