31907-86-5

Upstream product

• 4554-16-9 2,3-dibromopropionitrile 
• 100-46-9 benzylamine 

Downstream Products

• 159789-11-4 N-<<1-(4-acetylphenyl)-3-benzyl-2-oxoimidazolidin-4-yl>methyl>acetamide 
• 928118-73-4 (R)-N²-benzyl-N¹-tert-butoxycarbonyl-3-methoxypropane-1,2-diamine 
• 928118-61-0 (S)-2-benzylamino-3-methoxypropanamide 
• 928118-69-8 (R)-N²-benzyl-3-methoxypropane-1,2-diamine 
• 88286-11-7 2-N-benzylamino-3-fluoropropinonitrile 
• 88286-30-0 3-N-benzylamino-2-fluoropropinonitrile 
• 159789-10-3 1-(4-acetylphenyl)-3-(benzyl)-2-oxo-4-imidazolidine-4-carbonitrile 
• 94215-81-3 N-benzyl-2-bromo-β-alanine nitrile; hydrobromide 

Relevant academic research and scientific papers

Synthesis and Antimicrobial Activity of Oxazolidin-2-ones and Related Heterocycles

A series of 5-membered heterocycles, structurally related to the known antibacterial oxazolidin-2-ones 1, have been prepared by modifying the model compound 1a at the 1-, 2-, 2'- and 3-positions.The antibacterial activity of compound 1a was strongly affec

N-Substituted aziridine-2-carboxylic acid derivatives and their immuno-stimulation compositions and methods

A 2-cyanaziridine derivative of the formula STR1 wherein R' is a straight-chained or branched, saturated or mono- or polyunsaturated aliphatic hydrocarbon radical with up to 8 carbon atoms, which is substituted by an aromatic nitrogen-containing heterocyclic radical with 5 or 6 ring-members and 1, 2 or 3 nitrogen atoms optionally substituted by halogen, alkoxy with up to 8 carbon atoms, alkyl with up to 8 carbon atoms, hydroxyl, carbalkoxy with up to 9 carbon atoms, carbamoyl, dialkylamino the alkyl moieties of which having up to 8 carbon atoms, cycloalkylamino, the cycloalkyl moiety having 3-10 carbon atoms, acetylamino, nitro, cyano, acetyl, alkylthio with up to 8 carbon atoms, alkylsulphinyl with up to 8 carbon atoms, alkylsulphonyl with up to 8 carbon atoms, sulphamoyl, phenyl, trifluoromethyl, phenoxy, acetoxy or methylenedioxy; or a pharmacologically acceptable salt thereof, exhibits immune stimulating activity.

N-Substituted aziridine-2-carboxylic acid derivatives for immuno stimulation

Aziridine-2-carboxylic acid derivatives of the formula STR1 wherein X is a carboxyl, nitrile, alkoxycarbonyl or carbamoyl group, and R and R1 are various organic radicals, or pharmacologically acceptable salts thereof, exhibit marked immunostimulant activity, especially in conjunction with added chemotherapeutic agents such as a penicillin, a cephalosporin, a nitrofuran or chloramphenicol. Those compounds are new where X is a cyano group or an alkoxycarbonyl radical and R1 is a hydrogen atom, but R' is not an unsubstituted alkyl radical or an alkyl radical substituted by hydroxyl, alkoxy, dialkylamino, phenyl, 4-chlorophenyl or 4-methoxyphenyl or a vinyl radical substituted by a phenyl or methyl radical, or a cycloalkyl radical, a phenyl a 4-chlorophenyl, a 4-methoxyphenyl, an s-triazinyl or a pyridinyl radical; or where X is a carbamoyl group and R1 is a hydrogen atom, R' is not an unsubstituted cyclohexyl, alkyl or benzyl radical; or where X is a cyano group or an alkoxycarbonyl radical and R1 is a phenyl radical, R' is not an isopropyl, cyclohexyl, phenyl, benzyl or p-chlorobenzyl radical; or where R1 is a methyl radical, R1 is not a benzyl, p-chloro- or p- methoxybenzyl radical.