5957-17-5 Usage
Uses
Used in Organic Synthesis:
(2-HYDROXYETHYL)TRIETHYLAMMONIUM IODIDE is used as a phase-transfer catalyst for facilitating various organic reactions. Its hydrophilic nature and ability to transfer reactants between phases make it effective in promoting chemical transformations.
Used in Pharmaceutical Production:
In the pharmaceutical industry, (2-HYDROXYETHYL)TRIETHYLAMMONIUM IODIDE is used as a catalyst in the synthesis of various drugs. Its role in organic reactions contributes to the production of pharmaceuticals with improved efficiency and selectivity.
Used in Agrochemical Production:
Similarly, in agrochemical manufacturing, (2-HYDROXYETHYL)TRIETHYLAMMONIUM IODIDE serves as a phase-transfer catalyst, aiding in the synthesis of agrochemicals with enhanced yield and purity.
Used in Fine Chemicals Production:
(2-HYDROXYETHYL)TRIETHYLAMMONIUM IODIDE is also utilized in the production of fine chemicals, where its catalytic properties are harnessed to achieve precise and efficient synthesis processes.
Check Digit Verification of cas no
The CAS Registry Mumber 5957-17-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,9,5 and 7 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 5957-17:
(6*5)+(5*9)+(4*5)+(3*7)+(2*1)+(1*7)=125
125 % 10 = 5
So 5957-17-5 is a valid CAS Registry Number.
5957-17-5Relevant academic research and scientific papers
The importance of molecular parameters of quaternary ammonium salts in their antigibberellin (retardant) activity
Gafurov,Grigor'ev,Proshin,Chistyakov,Martynov,Zefirov
, p. 592 - 598 (2007/10/03)
The importance of six theoretically calculated molecular parameters in the antigibberellin (retardant) activity of quaternary ammonium salts is studied using a regression analysis. A bioassay system based on cell culture of fungus Gibberella fujikuroi is used to determine the activity. In the case of N,N,N-trimethyl-N-(2-hydroxyethyl)ammonium chloride (choline) and N,N,N-triethyl-N-(2-hydroxyethyl)ammonium chloride (N,N,N-triethylcholine) derivatives with linear structure, the polarizability, proton acceptor activity, and lipophilicity of these compounds exert the largest effect on the antigibberellin activity. The antigibberellin activity of more sterically hindered N,N-dialkylpiperidinium salts was mainly defined by the steric parameter, while the polarizability, proton acceptor activity, and (through them) lipophilicity exert a lesser effect. Other parameters are of minor importance for the three groups of compounds studied.
