24571-98-0 Usage
Chemical class
Spiro compounds These are molecules that contain two non-adjacent carbon atoms with a shared single bond.
Structure
Cyclic ketone with a nitrogen atom The presence of a nitrogen atom in the ring structure gives 1-Azaspiro[3.5]nonan-2-one unique properties and potential applications.
Potential applications
Pharmaceutical and agrochemical industries Due to its unique structure, 1-Azaspiro[3.5]nonan-2-one can be used as a building block for the synthesis of biologically active molecules.
Versatility
Organic synthesis The structure of 1-Azaspiro[3.5]nonan-2-one makes it a versatile starting material in organic synthesis.
Biological activity
Insecticidal and acaricidal properties 1-Azaspiro[3.5]nonan-2-one has been investigated for its potential insecticidal and acaricidal properties, making it an interesting target for further research and development in chemical biology and agricultural chemistry.
Research focus
Building block for synthesis 1-Azaspiro[3.5]nonan-2-one has been studied for its potential use as a building block for the synthesis of biologically active molecules, highlighting its importance in the development of new compounds with various applications.
Check Digit Verification of cas no
The CAS Registry Mumber 24571-98-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,5,7 and 1 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 24571-98:
(7*2)+(6*4)+(5*5)+(4*7)+(3*1)+(2*9)+(1*8)=120
120 % 10 = 0
So 24571-98-0 is a valid CAS Registry Number.
24571-98-0Relevant academic research and scientific papers
Barrett, Anthony G. M.,Fenwick, Ashley,Betts, Michael J.
, p. 299 - 301 (1983)
Condensation of the title isocyanates with olefins and subsequent dissolving-metal reduction (sulphonyl derivates) or chromatography on Florisil (trifluoroacetyl derivatives) gave several N-unsubstituted β-lactams including two 8-aza-2-oxabicyclooc
Acyl and Sulfonyl Isocyanates ib β-Lactam Synthesis
Barrett, Anthony G. M.,Betts, Michael J.,Fenwick, Ashley
, p. 169 - 175 (2007/10/02)
The preparation of β-lactams from the reactions of several acyl and sulfonyl activated isocyanates with alkenes was studied.Three compounds, (2,2,2-trichloroethoxy)sulfonyl, 2,2,2-trichloroethane sulfonyl, and trifluoroacetyl isocyanates, were shown to be
