162407-06-9 Usage
Chemical structure
A spiro compound containing a diazaspiro ring system and two 3,5-dimethoxyphenyl substituents.
Type of compound
Spiro compound.
Unique features
Presence of a diazaspiro ring system and two 3,5-dimethoxyphenyl groups.
Potential applications
Medicinal chemistry, specifically in the development of novel pharmaceuticals.
Relevance to synthetic chemists
Interesting target for synthetic chemists due to its complex and unique structure.
Importance in research
Researchers studying structure-activity relationships may find 1,4-Diazaspiro[4.5]deca-1,3-diene, 2,3-bis(3,5-dimethoxyphenyl)- valuable for their studies.
Biological activity
Its unique structural features may contribute to its biological activity and potential therapeutic properties.
Further research needed
More research is required to fully understand its medicinal potential and biological effects.
Check Digit Verification of cas no
The CAS Registry Mumber 162407-06-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,2,4,0 and 7 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 162407-06:
(8*1)+(7*6)+(6*2)+(5*4)+(4*0)+(3*7)+(2*0)+(1*6)=109
109 % 10 = 9
So 162407-06-9 is a valid CAS Registry Number.
162407-06-9Relevant academic research and scientific papers
Synthesis of an enantiopure fluorous 1,2-diphenyl-1,2-diaminoethane
Bayardon, Jerome,Sinou, Denis
, p. 425 - 428 (2007/10/03)
Enantiopure fluorous 1,2-diphenyl-1,2-ethanediamine bearing four fluorous ponytails and having 62.2% fluorine content has been prepared. Resolution of racemic 1,2-bis(3,5-dimethoxyphenyl)ethane-1,2-diamine with (-)-menthyl chloroformate followed by reduct
Convenient Routes to Symmetrical Benzils and Chiral 1,2-Diaryl-1,2-diaminoethanes, Useful Controllers and Probes for Enantioselective Synthesis
Corey, E. J.,Lee, Duck-Hyung,Sarshar, Sepehr
, p. 3 - 6 (2007/10/02)
Pathways for the diastereoselective preparation of chiral 1,2-diaryl-1,2-diaminoethanes from ArCOOH, ArCHO or ArBr are described.
