2089652-09-3 Usage
Uses
Used in Pharmaceutical Industry:
(S)-5-((benzyloxy)carbonyl)-5-azaspiro[2.4]heptane-7-carboxylic acid is used as a potential pharmaceutical agent for its unique structure and potential biological activity. Its application in this industry is driven by the need for novel compounds in drug discovery and development.
Used in Medicinal Chemistry Research:
In the field of medicinal chemistry, (S)-5-((benzyloxy)carbonyl)-5-azaspiro[2.4]heptane-7-carboxylic acid serves as a valuable building block for the synthesis of other complex molecules. Its role in this application is to facilitate the creation of new drugs and contribute to the advancement of pharmaceutical compounds.
Used in Drug Synthesis:
(S)-5-((benzyloxy)carbonyl)-5-azaspiro[2.4]heptane-7-carboxylic acid is utilized as an intermediate in the synthesis of various drugs. Its application in this area is due to its structural complexity and the possibility of its modification to produce a range of pharmaceutically relevant molecules.
Check Digit Verification of cas no
The CAS Registry Mumber 2089652-09-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 2,0,8,9,6,5 and 2 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 2089652-09:
(9*2)+(8*0)+(7*8)+(6*9)+(5*6)+(4*5)+(3*2)+(2*0)+(1*9)=193
193 % 10 = 3
So 2089652-09-3 is a valid CAS Registry Number.
2089652-09-3Relevant articles and documents
Synthesis of Spirocyclic Pyrrolidines: Advanced Building Blocks for Drug Discovery
Chalyk, Bohdan A.,Butko, Maryna V.,Yanshyna, Oksana O.,Gavrilenko, Konstantin S.,Druzhenko, Tetiana V.,Mykhailiuk, Pavel K.
, p. 16782 - 16786 (2017)
In the context of drug discovery, novel spirocyclic pyrrolidines have been synthesized in two steps from common three- to seven-membered-ring (hetero)alicyclic ketones. The key transformation is a reaction between an electron-deficient exocyclic alkene and an in situ generated N-benzyl azomethine ylide. The developed method has been used to synthesize the central diamine core of the known antibacterial agents Sitafloxacin and Olamufloxacin.
