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(4-Iodo-5-nitro-imidazol-1-yl)-acetic acid ethyl ester is a chemical compound with the molecular formula C6H7IN2O4. It is an ester derivative of (4-iodo-5-nitro-imidazol-1-yl)-acetic acid, where the hydroxyl group is replaced by an ethoxy group. (4-Iodo-5-nitro-imidazol-1-yl)-acetic acid ethyl ester is characterized by the presence of an imidazole ring, which is substituted with an iodo group at the 4-position and a nitro group at the 5-position. The ethyl ester group is attached to the carboxylic acid moiety, enhancing its lipophilic properties. This chemical is often used in the synthesis of pharmaceuticals and other organic compounds due to its unique structural features and reactivity.

96258-81-0

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96258-81-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 96258-81-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,6,2,5 and 8 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 96258-81:
(7*9)+(6*6)+(5*2)+(4*5)+(3*8)+(2*8)+(1*1)=170
170 % 10 = 0
So 96258-81-0 is a valid CAS Registry Number.

96258-81-0Upstream product

96258-81-0Downstream Products

96258-81-0Relevant academic research and scientific papers

Potential radiosensitizing agents. 7. 4(5)-Iodo-5(4)-nitroimidazole derivatives

Gupta,Larroquette,Agrawal,Grodkowski,Neta

, p. 987 - 991 (2007/10/02)

A series of 4(5)-iodo-5(4)-nitro-1-substituted-imidazoles has been synthesized and tested for their ability to selectively radiosensitize hypoxic Chinese hamster cells (V-79) to the lethal effect of radiation. The reaction of 4(5)-iodo-5(4)-nitroimidazole with 1,2-epoxy-3-methoxypropane and ethyl α-chloroacetate produced two isomeric products in each case, which were identified by their NMR spectra. The ethyl esters were further reacted with 3-picolylamine to produce corresponding amides. The 5-iodo-4-nitroimidazole-1-N-(3-picolyl)acetamide on further reaction with m-chloroperbenzoic acid produced the corresponding N-oxide. These compounds were generally more toxic to V-79 cells than the 2-nitroimidazole derivatives and were found to be more effective radiosensitizers in vitro. The 5-iodo-4-nitroimidazole derivatives were more efficient as sensitizers than the 4-iodo-5-nitroimidazole derivatives, and the sensitizing efficiency of this class of agents was found to have significant correlation with their partition coefficients.

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