53619-11-7 Usage
Uses
Used in Organic Synthesis:
1,4-Diazabicyclo[3.2.2]nonan-3-one is used as a catalyst in organic synthesis for its ability to accelerate various chemical reactions, enhancing the efficiency and selectivity of the processes involved.
Used in Pharmaceutical Industry:
1,4-Diazabicyclo[3.2.2]nonan-3-one is used as a reagent in the pharmaceutical industry for its role in the synthesis of complex organic molecules, contributing to the development of new drugs and medicinal compounds.
Used in Chemical Industry:
In the chemical industry, 1,4-Diazabicyclo[3.2.2]nonan-3-one is utilized as a catalyst for its high reactivity, enabling the production of a wide range of chemical products with improved yields and selectivity.
Used in Production of Fine Chemicals and Materials:
1,4-Diazabicyclo[3.2.2]nonan-3-one is employed in the production of fine chemicals and materials due to its unique structure and properties, which allow for the creation of specialized compounds with specific applications in various fields.
Check Digit Verification of cas no
The CAS Registry Mumber 53619-11-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,6,1 and 9 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 53619-11:
(7*5)+(6*3)+(5*6)+(4*1)+(3*9)+(2*1)+(1*1)=117
117 % 10 = 7
So 53619-11-7 is a valid CAS Registry Number.
InChI:InChI=1/C7H12N2O/c10-7-5-9-3-1-6(8-7)2-4-9/h6H,1-5H2,(H,8,10)
53619-11-7Relevant academic research and scientific papers
Microwave-assisted beckmann rearrangement: Convenient synthesis of 1,3-diaza-bicyclo[3.2.2]nonane
Curtis, Michael P.,Bunnelle, William H.,Pagano, Thomas G.,Gopalakrishnan, Murali,Faghih, Ramin
, p. 321 - 326 (2007/10/03)
Small heterocyclic amines such as 1,3-diaza-bicyclo[3.2.2]nonane are known to be key components of biologically active molecules. A convenient synthesis of this compound utilizing a key Beckmann rearrangement of (Z)-1-aza-bicyclo[2.2. 2]octan-3-one oxime (6) with conc. H2SO4 under microwave irradiation was achieved. The desired compound (1) was obtained in 20% yield overall. Copyright Taylor & Francis LLC.
