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N-(3-nitropyridin-4-yl)phenethylamine is a chemical compound with the molecular formula C15H14N4O3. It is an organic molecule that features a phenethylamine core, which is an ethylamine with a phenyl group attached. The compound is characterized by the presence of a 3-nitropyridin-4-yl group, which is a pyridine ring with a nitro group at the 3-position and a phenethylamine group attached to the 4-position. This structure gives the compound potential applications in various fields, such as pharmaceuticals and materials science, due to its unique electronic and steric properties. However, it is important to note that the specific uses and effects of N-(3-nitropyridin-4-yl)phenethylamine would depend on further research and characterization, as the information provided is limited to its chemical structure and does not include details on its reactivity, toxicity, or therapeutic potential.

2850-96-6

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2850-96-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2850-96-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,8,5 and 0 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 2850-96:
(6*2)+(5*8)+(4*5)+(3*0)+(2*9)+(1*6)=96
96 % 10 = 6
So 2850-96-6 is a valid CAS Registry Number.

2850-96-6Relevant academic research and scientific papers

Practical amination of nitropyridones by silylation

Singer, Robert A.,Dore, Michael

, p. 1261 - 1264 (2008)

A practical method for coupling nitropyridones (1) with primary amines by treatment with hexamethyldisilazane has been developed, avoiding the use of hazardous reagents such as POCl3. The activation of the pyridone by a nitro group is necessary for efficient coupling, leading to aminonitropyridines (3) in good yields. Regioisomers other than 3-nitro-4-pyridone (1) were found to be substantially less reactive but would undergo coupling with primary amines.

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