64002-82-0

Upstream product

• 93-98-1 N-phenyl benzoyl amide 
• 90473-80-6 Piperidine-1-carbothioic acid 1-chloro-1-phenyl-meth-(Z)-ylideneamide 
• 62-53-3 aniline 
• 110-89-4 piperidine 
• 20800-27-5 N-Phenyl-benzimidoyl-isothiocyanat 
• 4903-36-0 N-phenyl-benzimidoyl chloride 

Downstream Products

• 104355-35-3 N-[1-Morpholin-4-yl-1-piperidin-1-yl-meth-(Z)-ylidene]-N'-phenyl-benzamidine 
• 128652-28-8 N-{Phenyl-[(E)-phenylimino]-methyl}-piperidine-1-carboximidothioic acid ethyl ester 
• 133858-40-9 4-piperidino-1,2,5-triphenyl-1,6-dihydropyrimidin-6-one 
• 27582-35-0 N-(Di-piperidin-1-yl-methylene)-N'-phenyl-benzamidine 
• 133858-60-3 5-chloro-1,2-diphenyl-4-piperidino-1,6-dihydrpyrimidin-6-one 
• 128652-24-4 N-{Phenyl-[(E)-phenylimino]-methyl}-piperidine-1-carboximidothioic acid methyl ester 
• 1108616-29-0 2,3-diphenyl-5-piperidin-1-yl-3H-imidazole-4-carboxylic acid methyl ester 
• 27582-35-0 N-(di-piperidin-1-yl-methylene)-N'-phenyl-benzamidine 
• 128652-24-4 N-{Phenyl-[(E)-phenylimino]-methyl}-piperidine-1-carboximidothioic acid methyl ester 

Relevant academic research and scientific papers

Amidine derived 1,3-diazabuta-1,3-dienes as potential antibacterial and antifungal agents

Several 1-aryl-2-phenyl-4-piperidino-4-thioalkyl-1,3-diazabuta-1,3-dienes were prepared by the treatment of N-arylimino isothiocyanate with piperidine followed by S-alkylation with alkyl iodides in the presence of dry acetone and potassium hydroxide. The

REAKTIONEN AN NICKEL(II)KOORDINIERTEN N-ACYLTHIOHARNSTOFFEN MIT SAEURECHLORIDEN: EIN EINFACHER ZUGANG FUER NEUE THIOHARNSTOFF-DERIVATE

The reaction of transition metal coordinated N,N-dialkylsubstituted N'-benzoyl thioureas with electrophilic agents differs from the reaction of the non-coordinated ligands.The nickel(II)chelates 1 form with organic acid chlorides RCOCl the N',N'-diacylate