7541-76-6 Usage
Description
4-Formyl-N,N,N-trimethylbenzenaminium·iodide is a quaternary ammonium compound that features a positively charged nitrogen atom bonded to three methyl groups and a formyl group. This salt form of the compound includes an iodide ion as its counterion, which balances the positive charge on the ammonium group. It is widely recognized for its utility in organic synthesis, particularly in reactions involving the formation of carbon-carbon bonds and the alteration of organic molecules. 4-Formyl-N,N,N-trimethylbenzenaminium·iodide's unique properties and reactivity render it an indispensable tool in the realm of organic chemistry, where it aids in the synthesis of intricate molecules and pharmaceutical compounds.
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.
Check Digit Verification of cas no
The CAS Registry Mumber 7541-76-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,5,4 and 1 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 7541-76:
(6*7)+(5*5)+(4*4)+(3*1)+(2*7)+(1*6)=106
106 % 10 = 6
So 7541-76-6 is a valid CAS Registry Number.
InChI:InChI=1/C10H14NO/c1-11(2,3)10-6-4-9(8-12)5-7-10/h4-8H,1-3H3/q+1
7541-76-6Relevant articles and documents
Coacervation of dynamic covalent surfactants with polyacrylamides: Properties and applications
Zhao, Weiwei,Wang, Hua,Wang, Yilin
, p. 4178 - 4184 (2018/05/30)
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
Yuan, Hao,Zhou, Zhiming,Xiao, Jiangliang,Liang, Lixuan,Dai, Li
experimental part, p. 1874 - 1884 (2010/11/16)
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).
