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N-{2,5-bisnitrophenyl}acetamide is a chemical compound with the molecular formula C10H8N4O5. It is an organic compound that features a central acetamide group (-CONH2) attached to a 2,5-bisnitrophenyl moiety. The 2,5-bisnitrophenyl group consists of a benzene ring with two nitro groups (-NO2) at the 2nd and 5th positions. N-{2,5-bisnitrophenyl}acetamide is known for its potential applications in various fields, such as pharmaceuticals and chemical research, due to its unique structure and properties. It is important to handle N-{2,5-bisnitrophenyl}acetamide with care, as it may have hazardous effects and requires proper safety measures during its use and storage.

3717-73-5

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3717-73-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3717-73-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,7,1 and 7 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 3717-73:
(6*3)+(5*7)+(4*1)+(3*7)+(2*7)+(1*3)=95
95 % 10 = 5
So 3717-73-5 is a valid CAS Registry Number.

3717-73-5Relevant academic research and scientific papers

A Comparison of the Reactions of Some Ethyl N-Arylcarbamates with Those of the Corresponding Acetanilides. I. Nitration

Rosevear, Judi,Wilshire, John F. K.

, p. 723 - 733 (2007/10/02)

The reactions of some ethyl N-arylcarbamates and of the corresponding acetanilides towards 1 equiv. of sodium nitrate in concentrated sulfuric acid at 0-5 deg have been compared with one another and have been found to exhibit significant differences.Except in the case of the unsubstituted analogues, nitration of the carbamates was found to occur significantly more quickly than that of the acetanilides as shown by (i) a representative competitive nitration, and (ii) the fact the carbamates containing a nitro group are nitrated smoothly whereas the corresponding nitroacetanilides are slow to react.On the basis of competitive reactions, it is suggested that this difference in reactivity is due to steric factors.

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