65673-48-5 Usage
Uses
Used in Chemical Synthesis:
4-[2-(2-methoxyethoxy)ethoxy]aniline is used as an intermediate in the synthesis of dyes, pharmaceuticals, and other organic compounds for its ability to facilitate the formation of desired products in these industries.
Used in Catalysts for Polyurethane Synthesis:
4-[2-(2-methoxyethoxy)ethoxy]aniline is used as an effective catalyst in the synthesis of polyurethanes, enhancing the reaction process and improving the properties of the final product.
Used in Corrosion Inhibition:
4-[2-(2-methoxyethoxy)ethoxy]aniline is used as a corrosion inhibitor in metalworking fluids, helping to protect metal surfaces from degradation and extending the life of equipment and machinery.
Used in Various Industries:
4-[2-(2-methoxyethoxy)ethoxy]aniline is used across different industries, including chemical manufacturing, pharmaceutical development, and coatings and adhesives production, for its versatile properties and ability to improve product performance.
Safety Precautions:
Check Digit Verification of cas no
The CAS Registry Mumber 65673-48-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,6,7 and 3 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 65673-48:
(7*6)+(6*5)+(5*6)+(4*7)+(3*3)+(2*4)+(1*8)=155
155 % 10 = 5
So 65673-48-5 is a valid CAS Registry Number.
InChI:InChI=1/C11H17NO3/c1-13-6-7-14-8-9-15-11-4-2-10(12)3-5-11/h2-5H,6-9,12H2,1H3
65673-48-5Relevant academic research and scientific papers
Oligoindole-based foldamers with a helical conformation induced by chloride
Chang, Kyoung-Jin,Kang, Byung-Nam,Lee, Min-Hee,Jeong, Kyu-Sung
, p. 12214 - 12215 (2007/10/03)
As a new type of foldamers, oligoindoles containing 4, 6, and 8 indole rings were synthesized, and their folding properties were characterized by a combination of 1H NMR techniques and UV/visible titration experiments. When chloride was added, the NH signals of the oligoindoles were downfield shifted as a result of hydrogen-bond formation, and the aromatic signals were upfield shifted by stacking between two indoles. Moreover, the ROESY experiment provided definitive NOE evidence for the helical stacking in the presence of chloride. Finally, the UV/visible titration experiments demonstrated that the oligoindoles formed 1:1 complexes with chloride, and the association constants greatly increased with increasing the number of the indole NHs. These observations are all consistent with the fact that oligoindoles adopt a helical conformation when complexed with chloride by hydrogen-bonding interactions. Copyright
