16694-46-5

Usage

Uses

Used in Chemical Synthesis:
Ethyl Formimidate Hydrochloride is used as a building block for the preparation of s-triazines, 2,3:5,6-di-O-isopropylidene-αand -β-5-amino-4-ethoxycarbonyl or -carbamoyl-imidazole D-mannofuranosides. It plays a crucial role in the synthesis of complex organic compounds and pharmaceuticals.
Used in Pharmaceutical Industry:
Ethyl Formimidate Hydrochloride is used as a reactant in the synthesis of biologically active molecules, including Bredinin via amination of an acyclic precursor. ETHYL FORMIMIDATE HYDROCHLORIDE has therapeutic properties and is valuable in the development of new drugs.
Used in Antifungal Drug Synthesis:
In the pharmaceutical industry, Ethyl Formimidate Hydrochloride is also used as a reactant in the synthesis of Amidine conjugates of the ornithine moiety of an antifungal. This application highlights its importance in creating compounds with potential antifungal properties.
Used in Organic Chemistry Research:
Ethyl Formimidate Hydrochloride is utilized as a reactant involved in intermolecular cyclization and Mo-catalyzed asymmetric ring-closing metathesis for the synthesis of cyclid amides and amines. These processes are essential for the development of novel organic compounds with unique properties.
Used in Peptide Synthesis:
In the field of peptide chemistry, Ethyl Formimidate Hydrochloride is used in the synthesis of peptidic 1-cyanopyrrolidines. This application demonstrates its versatility in the creation of diverse peptide structures with potential biological activities.

InChI:InChI=1/C3H7NO/c1-2-5-3-4/h3-4H,2H2,1H3/b4-3+

Upstream product

• 64-17-5 ethanol 
• 74-90-8 hydrogen cyanide 
• 7647-01-0 hydrogenchloride 
• 60-29-7 diethyl ether 
• 77287-34-4 formamide 

Downstream Products

• 13529-27-6 2-(diethoxymethyl)furan 
• 6320-14-5 1,1′,3,3,3′,3′-hexamethylindocarbocyanine chloride 
• 122-51-0 orthoformic acid triethyl ester 
• 584-13-4 4-amino-1,2,4-triazole 
• 774-48-1 (diethoxymethyl)benzene 
• 126-84-1 2,2-diethoxypropane 
• 78070-34-5 1,4-cyclohexanedione bis(diethyl acetal) 
• 972-46-3 3-ethoxyandrosta-3,5-dien-17-one 
• 273-53-0 benzoxazole 
• 758-17-8 1-Methyl-1-formylhydrazid 
• 72964-09-1 4-(diphenylmethyl)-1-piperidinemethanimine hydrochloride 
• 124065-23-2 N-(iminomethyl)noratropine hydrochloride 
• 624-82-8 formamide oxime 
• 146464-48-4 ethyl formhydroximate 

Relevant academic research and scientific papers

METHOD FOR PREPARING 5-CHLORO-N-(METHYL)THIOPHEN-2-CARBOXAMIDE DERIVATIVE AND INTERMEDIATE USED THEREIN

Disclosed are: a method for preparing a 5-chloro-N-({(5S)-2-oxo-3-[4-(5,6-dihydro-4H-[1,2,4]triazin-1-yl)phenyl]-1,3-oxazolidin-5-yl}-methyl)thiophene-2-carboxamide derivative, which is a inhibitor of blood coagulation factor Xa, in a high purity and yiel

METHOD FOR PREPARING 5-CHLORO-N-({(5S)-2-OXO-3-[4-(5,6-DIHYDRO-4H-[1,2,4]TRIAZIN-1-YL)PHENYL]-1,3-OXAZOLIDIN-5-YL}METHYL)THIOPHEN-2-CARBOXAMIDE DERIVATIVE AND INTERMEDIATE USED THEREIN

Disclosed are : a method for preparing a 5-chloro-N-({(5S)-2-oxo-3-[4-(5,6-dihydro-4H-[1,2,4]triazin-1-yl)phenyl]-1,3-oxazolidin-5-yl}-methyl)thiophen-2-carboxamide derivative, which is a inhibitor of blood coagulation factor Xa, in a high purity and yiel

HETEROCYCLIC AMIDE COMPOUNDS AND PHARMACEUTICAL USE OF THE SAME

Heterocyclic amide compounds of the formula (I) STR1 wherein each symbol is as defined in the specification, pharmacologically acceptable salts thereof, pharmaceutical compositions thereof and pharmaceutical use thereof. The heterocyclic amide compounds and pharmacologically acceptable salts thereof of the present invention have superior inhibitory activity against chymase groups in mammals inclusive of human, and can be administered orally or parenterally. Therefore, they are useful as chymase inhibitors and can be effective for the prophylaxis and treatment of various diseases caused by chymase, such as those caused by angiotensin II.

A synthesis of adenine. The incorporation of isotopes of nitrogen and carbon

Various synthests of adenine have been investigated and a satisfactory procedure for the introduction of isotopes of nitrogen and carbon has been developed. 'The preparation from isotopic carbon of cyanoacetamide and malononitrile is described.