49744-35-6 Usage
Uses
Used in Cosmetics and Personal Care Industry:
2-(2-methoxyethoxy)ethyl anthranilate is used as a UV filter for its ability to absorb and block UV rays, thereby protecting the skin from sun damage and reducing the risk of sunburn and skin cancer. It is known for its high photostability and efficacy in providing broad-spectrum UV protection.
Used in Sunscreen Products:
2-(2-methoxyethoxy)ethyl anthranilate is used as an active ingredient in sunscreens for its ability to protect the skin from harmful UV rays. It is considered safe for use in cosmetics and personal care products, making it a popular ingredient in many sunscreens and other skin care products.
Check Digit Verification of cas no
The CAS Registry Mumber 49744-35-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,9,7,4 and 4 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 49744-35:
(7*4)+(6*9)+(5*7)+(4*4)+(3*4)+(2*3)+(1*5)=156
156 % 10 = 6
So 49744-35-6 is a valid CAS Registry Number.
InChI:InChI=1/C12H17NO4/c1-15-6-7-16-8-9-17-12(14)10-2-4-11(13)5-3-10/h2-5H,6-9,13H2,1H3
49744-35-6Relevant 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
