889675-06-3 Usage
Uses
Used in Pharmaceutical Research and Development:
1-(4-(Benzyloxy)-1H-indol-2-yl)ethanol is used as a chemical intermediate for the synthesis of various pharmaceutical compounds. Its unique structure, which includes an indole ring and a benzyloxy group, may contribute to the development of new drugs with novel mechanisms of action.
Used in Organic Synthesis:
In the field of organic synthesis, 1-(4-(Benzyloxy)-1H-indol-2-yl)ethanol serves as a valuable building block for creating more complex organic molecules. Its functional groups can be further modified or used as a starting point for the synthesis of a wide range of compounds with potential applications in various industries, including pharmaceuticals, agrochemicals, and materials science.
Check Digit Verification of cas no
The CAS Registry Mumber 889675-06-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,8,9,6,7 and 5 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 889675-06:
(8*8)+(7*8)+(6*9)+(5*6)+(4*7)+(3*5)+(2*0)+(1*6)=253
253 % 10 = 3
So 889675-06-3 is a valid CAS Registry Number.
889675-06-3Relevant academic research and scientific papers
The first potent inhibitor of mammalian group X secreted phospholipase A2: Elucidation of sites for enhanced binding
Smart, Brian P.,Oslund, Rob C.,Walsh, Laura A.,Gelb, Michael H.
, p. 2858 - 2860 (2007/10/03)
Using the X-ray structure of human group X secreted phospholipase A 2 (hGX), we carried out structure-based design of indole-based inhibitors and prepared the compounds using a new synthetic route. The most potent compound inhibited hGX and the mouse orthologue with an IC50 of 75 nM. This compound is the most potent hGX inhibitor reported to date and was also found to inhibit a subset of the other mouse and human SPLA 2S.
