926-72-7

Usage

Uses

Used in Organic Synthesis:
Amidinouronium chloride is used as a synthetic intermediate for the preparation of various organic compounds. Its unique structure allows it to be a valuable component in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Pharmaceutical Industry:
Amidinouronium chloride is used as a key building block in the synthesis of pharmaceutical compounds. Its reactivity and versatility make it an essential component in the development of new drugs and therapeutic agents.
Used in Agrochemical Industry:
Amidinouronium chloride is used as a precursor in the synthesis of agrochemicals, such as pesticides and herbicides. Its unique properties enable the development of more effective and targeted agrochemicals.

InChI:InChI=1/C2H6N4O.ClH/c3-1(4)6-2(5)7;/h(H6,3,4,5,6,7);1H

Upstream product

• 127099-85-8 dicyandiamide 

Downstream Products

• 141-83-3 1-carbamoylguanidine 

Relevant academic research and scientific papers

Crystal Structure and Spectroscopic Analyses of Guanylurea Hydrochloride. Evidence of the Influence of Hydrogen Bonding on the ?-Electron Delocalization

The crystal structure, and a complete vibrational analysis by FTIR and Raman spectra, of guanylurea hydrochloride are presented.The crystallographic results show a pronounced ?-electron delocalization on the cation and the presence of strong intra- and inter-molecular hydrogen bonding interactions between amino groups belonging to the guanidine moiety and the carbonyl oxygen of the ureic group.This arrangement gives rise to a polymer-like structure, in which the guanylurea cation chains are laterally hydrogen bonded by Cl- anions and water molecules.The UV-VIS reflectance spectra are in agreement with the hypothesis of the existence of hydrogen bonding charge transfer complexes in the solid state.Other spectroscopic techniques, such as FTIR and Raman, have been employed to support the crystal data and to investigate the vibrational assignments for this compound.

Amidinoureas substituted in both the urea and amidino nitrogen positions

A method of inducing blood pressure reduction in humans and mammals by administering 2,6-disubstituted phenyl N-alkyl amidinoureas in which the phenyl ring is additionally substituted by a hydroxy, alkoxy, aralkoxy, alkenyloxy, alkynyloxy, acyloxy or halo acyloxy group and a novel class of amidinourea compounds having pharmaceutical uses, including blood pressure lowering activity.

Substituted phenyl amidinoureas

This invention relates to a method of lowering blood pressure in humans and mammals using 2,6-disubstituted phenyl amidinoureas in which the phenyl ring is additionally substituted by a hydroxy, alkoxy, aralkoxy, alkenyloxy, alkynyloxy, haloacyloxy, or acyloxy group and to novel 2,6-disubstituted phenyl amidinoureas which possess pharmaceutical properties, including blood pressure lowering activity.