70974-47-9 Usage
Uses
Used in Surfactant Applications:
1-(pyrrolidin-1-yl)tetradecan-1-one is used as a surfactant due to its long hydrophobic chain and polar functional group, which can lower the surface tension of liquids and stabilize emulsions or foams.
Used in Organic Synthesis:
1-(pyrrolidin-1-yl)tetradecan-1-one is used as a building block or intermediate in the synthesis of more complex organic molecules, leveraging its ketone and pyrrolidine functionalities for chemical reactions.
Used in Pharmaceutical Industry:
1-(pyrrolidin-1-yl)tetradecan-1-one is used as a pharmaceutical agent or precursor for the development of new drugs, potentially owing to its unique structural features that may interact with biological targets.
Used in Materials Science:
1-(pyrrolidin-1-yl)tetradecan-1-one is used in the development of new materials, such as polymers or coatings, where its surfactant properties and chemical reactivity could be harnessed to improve material properties or performance.
Check Digit Verification of cas no
The CAS Registry Mumber 70974-47-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,0,9,7 and 4 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 70974-47:
(7*7)+(6*0)+(5*9)+(4*7)+(3*4)+(2*4)+(1*7)=149
149 % 10 = 9
So 70974-47-9 is a valid CAS Registry Number.
70974-47-9Relevant academic research and scientific papers
Reaction of N-Nitroso- and N-Nitro-N-alkylamides with Amines
Garcia, Jordi,Gonzalez, Javier,Segura, Ramon,Urpi, Felix,Vilarrasa, Jaume
, p. 3322 - 3327 (2007/10/02)
Several N-nitroso- and N-nitrocarboxamides have been characterized by 1H and 13C NMR spectroscopy.These compounds react with ammonia and aliphatic amines to afford mainly carboxamides of general formula RCONH2, RCONHR', or RCONR'R''.N-Nitrosocarboxamides and aromatic amines give poor yields of RCONHAr; by contrast, N-nitrocarboxamides and aromatic amines lead to RCONHAr in good yields.The higher thermal stability of the N-nitroamides as compared to N-nitrosoamides is advantageous in this connection; nevertheless, the principal advantage of the NNO2 group appears to be that it activates the nucleophilic attack to the carbonyl of the amide function more than the NNO group, as has been demonstrated by competitive experiments.The reaction of N-nitroso- and N-nitro-N-methylsulfonamides with ammonia and diethylamine has been studied as well; whereas N-methyl-N-nitro-p-toluenesulfonamide reacts as N-nitrocarboxamides, transnitration is predominant with N-methyl-N-nitroso-p-toluenesulfonamide.
