13230-44-9 Usage
Type of compound
Derivative of imidazole
Imidazole structure
Five-membered ring containing three carbon atoms and two nitrogen atoms
Additional groups
Benzyl group and methyl group
Nitro group
Attached to the imidazole ring
Classification
Nitroimidazole compound
Pharmaceutical use
Anti-infective agents
Target infections
Protozoan and bacterial infections
Potential applications
Medicine
Research focus
Antimicrobial and antiprotozoal properties
Check Digit Verification of cas no
The CAS Registry Mumber 13230-44-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,2,3 and 0 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 13230-44:
(7*1)+(6*3)+(5*2)+(4*3)+(3*0)+(2*4)+(1*4)=59
59 % 10 = 9
So 13230-44-9 is a valid CAS Registry Number.
13230-44-9Relevant academic research and scientific papers
Regioselective Alkylation of 4(5)-Nitro-1H-Imidazoles in Acidic Media: Study of Temperature Effects
Rao, A. K. S. Bhujanga,Rao, C. Gundu,Singh, B. B.
, p. 2399 - 2402 (2007/10/02)
Alkylation of 4(5)-nitro-1H-imidazoles in acidic media with reactive alkylating agents such as benzyl chloride and allyl bromide resulted in the predominant formation of the 5-nitro isomers at lower temperatures (75 deg C) and the 4-nitro isomers at higher temperatures (140 deg C).With less reactive alkylating agents, only the 5-nitro isomers were produced irrespective of temperature.The mechanism was shown to involve quaternization of the initially formed 1-alkyl-5-nitro-1H-imidazoles followed by preferential dealkylation to yield the thermodynamically more stable 4-nitro-1H-imidazoles.
