75988-63-5 Usage
Explanation
The molecular formula represents the number of atoms of each element present in a molecule of the compound.
Explanation
The compound has a heterocyclic ring structure with an amine functional group attached.
Explanation
1,4-Dioxaspiro[4.4]non-8-en-7-amine(9CI) may be used as a starting material or intermediate in the synthesis of other organic compounds.
Explanation
The compound's chemical structure suggests it may have potential applications in the development of pharmaceuticals and agrochemicals, although further research is needed.
Explanation
Due to the lack of extensive research, the compound's safety profile is not well known, and it should be handled with care and proper safety protocols.
Explanation
Additional research and testing are required to gain a comprehensive understanding of 1,4-Dioxaspiro[4.4]non-8-en-7-amine(9CI) and to determine its potential applications and safety profile.
Chemical structure
Heterocyclic amine derivative
Potential intermediate
Synthesis of other organic compounds
Applications
Pharmaceutical and agrochemical industries
Research status
Not widely studied
Safety concerns
Potential hazards and toxicological properties not well established
Further research
Needed to understand properties and potential uses
Check Digit Verification of cas no
The CAS Registry Mumber 75988-63-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,5,9,8 and 8 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 75988-63:
(7*7)+(6*5)+(5*9)+(4*8)+(3*8)+(2*6)+(1*3)=195
195 % 10 = 5
So 75988-63-5 is a valid CAS Registry Number.
75988-63-5Relevant academic research and scientific papers
Synthesis of 2,4-Diazabicyclooctane-3,7-diones and 3-Thioxo-2,4-diazabicyclooctan-7-one by an Intramolecular Michael-type Reaction. Stability of 2,4 Diaza-, 4-Oxa-2-aza-, and 4-Thia-2-aza-bicyclooctane-3,7-diones
Harris, C. John
, p. 2497 - 2502 (2007/10/02)
Novel 2,4-diazabicyclooctane-3,7-diones (10) have been prepared by an intramolecular Micael-type cyclisation.The analogous 3-thioxo-2,4-diazabicyclooctan-7-one system (20) is obtained by base-catalysed retro-Michael reaction of the less stable 3-arylimino-2-thia-4-azabicyclooctan-7-one isomer (19).The 2-aza-4-oxabicyclooctane-3,7-dione system (17) is shown to be very unstable to base, fragmenting via the carbamic acid to give carbon dioxide and a 4-N-substituted cyclopent-2-enone (11).The relative stability to base of these bicyclic systems is correlated with their structure.
