70974-47-9

Basic information

• Product Name: 1-(pyrrolidin-1-yl)tetradecan-1-one
• CAS NO: 70974-47-9
• Molecular Formula: C₁₈H₃₅NO
• Molecular Weight: 281.4766
• Mol File: 70974-47-9.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 403.3°C at 760 mmHg
• Flash Point: 164.6°C
• Density: 0.91g/cm³
• Vapor Pressure: 1.02E-06mmHg at 25°C
• Refractive Index: 1.473
• CAS DataBase Reference: 1-(pyrrolidin-1-yl)tetradecan-1-one(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(pyrrolidin-1-yl)tetradecan-1-one(70974-47-9)
• EPA Substance Registry System: 1-(pyrrolidin-1-yl)tetradecan-1-one(70974-47-9)

Safety Data

• Hazardous Substances Data: 70974-47-9(Hazardous Substances Data)

Usage

General Description

1-(pyrrolidin-1-yl)tetradecan-1-one is a chemical compound with the molecular formula C18H35NO. It is a ketone derivative with a pyrrolidine group attached to a tetradecane chain. 1-(pyrrolidin-1-yl)tetradecan-1-one is likely to have surfactant properties due to its long hydrophobic chain and polar functional group. It may also have potential applications in the field of organic synthesis, pharmaceuticals, and materials science. Further research and testing are needed to fully understand the properties and potential uses of 1-(pyrrolidin-1-yl)tetradecan-1-one.

Upstream product

• 123-75-1 pyrrolidine 
• 91083-86-2 N-Ethyl-N-nitrosomyristamide 
• 91084-04-7 N-ethyltetradecanamide 

Downstream Products

• 74673-29-3 1-tetradecylpyrrolidine 

Relevant articles and documents

Reaction of N-Nitroso- and N-Nitro-N-alkylamides with Amines

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.