7541-76-6

Basic information

• Product Name: 4-Formyl-N,N,N-trimethylbenzenaminium·iodide
• Synonyms: 4-Formyl-N,N,N-trimethylbenzenaminium·iodide;(4-formylphenyl)-trimethylammonium iodide;(4-formylphenyl)-trimethyl-ammonium iodide;(4-formylphenyl)-trimethylazanium iodide;(4-methanoylphenyl)-trimethyl-azanium iodide;(p-Formylphenyl)trimethylammonium iodide;4-Formylphenyltrimethylammonium iodide;AMMONIUM, (p-FORMYLPHENYL)TRIMETHYL-, IODIDE
• CAS NO: 7541-76-6
• Molecular Formula: C₁₀H₁₄NO*I
• Molecular Weight: 291.13
• Mol File: 7541-76-6.mol
• Article Data: 3

Chemical Properties

• Boiling Point: °Cat760mmHg
• Flash Point: °C
• Appearance: /
• Density: g/cm³
• CAS DataBase Reference: 4-Formyl-N,N,N-trimethylbenzenaminium·iodide(CAS DataBase Reference)
• NIST Chemistry Reference: 4-Formyl-N,N,N-trimethylbenzenaminium·iodide(7541-76-6)
• EPA Substance Registry System: 4-Formyl-N,N,N-trimethylbenzenaminium·iodide(7541-76-6)

Safety Data

• Hazardous Substances Data: 7541-76-6(Hazardous Substances Data)

Usage

General Description

4-Formyl-N,N,N-trimethylbenzenaminium·iodide is a chemical compound that is commonly used in organic synthesis. It is a salt form of a quaternary ammonium compound, containing a positively charged nitrogen atom surrounded by three methyl groups and a formyl group. The iodide ion acts as a counterion in the compound, balancing the positive charge on the ammonium group. 4-Formyl-N,N,N-trimethylbenzenaminium·iodide is often utilized as a reagent in various chemical reactions, particularly in the formation of carbon-carbon bonds and the modification of organic molecules. Its properties and reactivity make it a valuable tool in the field of organic chemistry for the creation of complex molecules and pharmaceutical compounds.

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 
• 115109-21-2 4-[18F]fluorobenzaldehyde 

Relevant articles and documents

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

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).