1787-64-0 Usage
Structure
Imidazole ring with a carboxamide group and a nitrophenyl group attached
Common uses
Anti-fungal agent with broad-spectrum activity against various fungi
Mode of action
Interferes with fungal cell wall synthesis, leading to cell destruction
Potential uses
Anti-cancer agent, under investigation for cancer treatment
Safety precautions
May be harmful if ingested or inhaled, can cause skin and eye irritation, handle with caution.
Check Digit Verification of cas no
The CAS Registry Mumber 1787-64-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,7,8 and 7 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1787-64:
(6*1)+(5*7)+(4*8)+(3*7)+(2*6)+(1*4)=110
110 % 10 = 0
So 1787-64-0 is a valid CAS Registry Number.
1787-64-0Relevant academic research and scientific papers
Nitroimidazoles: Part XII - Reaction of 1-Methyl-5-nitroimidazoles with Acid Chlorides
Nair, M. D.,Sudarsanam, V.,Desai, J. A.
, p. 1027 - 1029 (2007/10/02)
The aroylation of 1-methyl-5-nitroimidazole with aroyl chlorides in the presence of triethylamine leads to 2-aroyl-1-methyl-5-nitroimidazole(I).Beckmann rearrangement of the corresponding oximes (II) yield the anilides (III) as normal Beckmann products.Aroylation of I with p-nitrobenzoyl chloride yields besides the normal derivative (IVa), a minor product (IVB) formed by the attack of a second molecule of the nitroimidazole on the carbonyl carbon.Methyloxalyl chloride similarly yields two products, the major one being the 2-carbomethoxy derivative (VIA).
