131475-54-2

Usage

General Description

1H-Imidazole-1-carboxamide, N-2-propenyl-(9CI) is a chemical compound with the molecular formula C7H9N3O. The compound is an imidazole derivative, which is a five-membered heterocyclic ring containing two nitrogen atoms. The presence of the 2-propenyl group suggests that it contains a propenyl group attached to the nitrogen atom of the imidazole ring. 1H-Imidazole-1-carboxamide,N-2-propenyl-(9CI) may have potential applications in the pharmaceutical or organic synthesis industries, as imidazole derivatives are known to have various biological activities and are widely used as building blocks in the synthesis of pharmaceuticals and agrochemicals. Further research is necessary to determine the specific properties and potential uses of this chemical compound.

Upstream product

• 107-11-9 1-amino-2-propene 
• 530-62-1 1,1'-carbonyldiimidazole 

Downstream Products

• 1003010-79-4 acetophenone N-allylcarbamoyl oxime 

Relevant academic research and scientific papers

HETEROCYCLIC CARBOXYLIC ACID ESTER DERIVATIVE

The present invention provides a blood glucose elevation inhibitor having a serine protease inhibitory action, which is a novel therapeutic or prophylactic agent for obesity. A compound represented by the following formula (I) wherein each symbol is as described in the specification, or a pharmaceutically acceptable salt thereof.

Dissociation or cyclization: Options for a triad of radicals released from oxime carbamates

A set of oxime carbamates having N-alkyl and N,N-dialkyl substituents were prepared via carbonyldiimidazole intermediates. It was shown by EPR spectroscopy that they underwent clean homolysis of their N-O bonds upon UV photolysis. During photolysis of acetophenone O-allylcarbamoyl oxime, the corresponding oxazolidin-2-onylmethyl radical was detected by EPR spectroscopy, providing the first evidence that N-monosubstituted carbamoyloxyl radicals can hold their structural integrity. N,N-Disubstituted carbamoyloxyl radicals dissociated rapidly at the lowest accessible temperatures. Above room temperature, both types of oxime carbamate acted as selective new precursors for aminyl and iminyl radicals. Rate parameters were measured for 5-exo cyclization of N-benzyl-N-pent-4-enylaminyl radicals; the rate constant was smaller than for C-centered and O-centered analogues. Oxime carbamates derived from the volatile diethylamine afforded aryliminyl radicals that proved convenient for phenanthridine preparations.