3535-16-8

Upstream product

• 6780-13-8 1,2-ethanediamine monohydrate 
• 622-24-2 2-phenylethyl chloride 
• 107-15-3 ethylenediamine 
• 103-63-9 1-phenyl-2-bromoethane 

Downstream Products

• 5700-52-7 N-benzyl-N'-phenethyl-ethylenediamine 
• 6248-18-6 N-phenethyl-N'-veratryl-ethylenediamine 
• 107235-84-7 N-(Phenylethyl)-N'-benzoylethylenediamine Hydrochloride 
• 107235-85-8 N-(Phenylethyl)-N'-cyclohexylcarbonylethylenediamine Hydrochloride 

Relevant academic research and scientific papers

Preparation of ternary platinum(II) complexes with N-(ω-phenylalkyl)- 1,2-ethanediamine and 2,2′-dipyridine and the effect of the methylene chain length of the N-(ω-phenylalkyl)-1,2-ethanediamine in the complexes on intermolecular interactions with various arylsulfonates

A series of ternary complexes comprised of platinum(II), 2,2′-dipyridine, and N-(ω-phenylalkyl)-1,2-ethanediamine was prepared by varying the number (n) of methylene chain carbons between the phenyl group and one of the amino groups of 1,2-ethanediamine. NMR measurements indicated that intramolecular stacking occurred for n=1 and intermolecular stacking occurred for n=3 for several of the aryl sulfonates.

ALPHA HYDROXY AMIDES

The present invention relates to alpha hydroxy amides including compounds of formula (I) and related compounds and their use in the prophylaxis and treatment of inflammatory disorders and diseases, wherein T1, T2, W and Rw has the meaning given in claim 1.

Synthesis of 6- to 10-membered ring (E)- hydroxyiminohydroazaazoniabenzocycloalkenes derivative from cyclization of 2-nitromethylene-1-(ω-phenylalkyl)imidazolidine or 2-nitromethylene-1- (ω-phenylalkyl)hexahydropyrimidine in trifluoromethanesulfonic acid

In trifluoromethanesulfonic acid, 2-nitromethylene-1-(ω-phenylalkyl) imidazolidine or 2-nitromethylene-1-(ω-phenylalkyl)hexahydropyrimidine derivatives undergo an intramolecular cyclization to afford (E)- hydroxyiminohydroazaazoniabenzocycloalkenes, in th