56674-87-4 Usage
Description
2-Adamantone-5-carboxylic acid is an organic compound characterized by its adamantane core and carboxylic acid functional group. It is a white crystalline solid with a unique molecular structure that contributes to its diverse applications in various industries.
Uses
Used in Pharmaceutical Industry:
2-Adamantone-5-carboxylic acid is used as a reactant for the synthesis of potent inhibitors targeting the drug-resistant mutant of Influenza A. Its unique structure allows for the development of effective antiviral agents that can combat resistant strains of the virus.
Used in Pharmaceutical Industry (continued):
2-Adamantone-5-carboxylic acid is also used as a starting material for the synthesis of Saxagliptin impurities. Saxagliptin is a medication used to treat type 2 diabetes, and the synthesis of its impurities is essential for ensuring the safety and efficacy of the drug.
Check Digit Verification of cas no
The CAS Registry Mumber 56674-87-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,6,7 and 4 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 56674-87:
(7*5)+(6*6)+(5*6)+(4*7)+(3*4)+(2*8)+(1*7)=164
164 % 10 = 4
So 56674-87-4 is a valid CAS Registry Number.
InChI:InChI=1/C11H14O3/c12-9-7-1-6-2-8(9)5-11(3-6,4-7)10(13)14/h6-8H,1-5H2,(H,13,14)
56674-87-4Relevant articles and documents
Alkane oxidation catalysed by a self-folded multi-iron complex
Mettry, Magi,Moehlig, Melissa Padilla,Gill, Adam D.,Hooley, Richard J.
, p. 120 - 128 (2016/11/09)
A preorganised ligand scaffold is capable of coordinating multiple Fe(II) centres to form an electrophilic CH oxidation catalyst. This catalyst oxidises unactivated hydrocarbons including simple, linear alkanes under mild conditions in good yields with selectivity for the oxidation of secondary CH bonds. Control complexes containing a single metal centre are incapable of oxidising unstrained linear hydrocarbons, indicating that participation of multiple centres aids the CH oxidation of challenging substrates.