175166-50-4 Usage
Uses
Used in Pharmaceutical Research and Development:
(3aS,8aR)-(8,8a-Dihydro-3aH-indeno[1,2-d]oxazol-2-yl)-acetonitrile is used as a building block for the synthesis of biologically active molecules, contributing to the development of novel drugs and therapeutic agents. Its unique structure and properties make it a valuable component in the creation of pharmaceutical intermediates.
Used in Drug Synthesis:
In the pharmaceutical industry, (3aS,8aR)-(8,8a-Dihydro-3aH-indeno[1,2-d]oxazol-2-yl)-acetonitrile is used as a key intermediate in the synthesis of various medical compounds. Its potential applications in the treatment of different medical conditions make it an important substance for researchers in medicinal chemistry.
Used in Drug Development:
(3aS,8aR)-(8,8a-Dihydro-3aH-indeno[1,2-d]oxazol-2-yl)-acetonitrile is employed in drug development for its potential to contribute to the creation of new therapeutic agents. Its presence in the synthesis process can lead to the discovery of innovative treatments for a range of medical conditions, making it a compound of interest to pharmaceutical researchers.
Check Digit Verification of cas no
The CAS Registry Mumber 175166-50-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,5,1,6 and 6 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 175166-50:
(8*1)+(7*7)+(6*5)+(5*1)+(4*6)+(3*6)+(2*5)+(1*0)=144
144 % 10 = 4
So 175166-50-4 is a valid CAS Registry Number.
175166-50-4Relevant academic research and scientific papers
Application of a Ritter-type reaction to the synthesis of chiral indane-derived C2-symmetric bis(oxazolines)
Davies, Ian W.,Senanayake, Chris H.,Larsen, Robert D.,Verhoeven, Thomas R.,Reider, Paul J.
, p. 813 - 814 (2007/10/03)
Bis(oxazolines) 4, 6, 8, 9, 10, and 11 are prepared in a highly regio- and diastereo-selective manner from dinitriles and indanediol 3 in a Ritter-type reaction initiated by trifluoromethanesulfonic acid.
