“…The 1-[2-(dimethylamino)ethyl]-3-undecylurea was prepared using a similar procedure as was used for the 1-cyclohexyl-3-[2-(dimethylamino)ethyl] urea [48] as follows. Into the ice-cooled stirred solution of 1-isocyanotoundecane (10 g, 35 mmol) in 25 mL of dry acetonitrile, 2.1 g (24 mmol) of 2-(N, N-dimethyl)ethane-1,2-diamine were added dropwise during 15 minutes.…”
Section: Preparation Of 1-[2-(dimethylamino) Ethyl]-3-undecylureamentioning
with the maximum antimicrobial activity found at the spacer length of 6 CH2 groups for bacteria and 8 CH2 groups for fungi. This is related to a different composition of cell membrane of the used microorganisms.
“…The 1-[2-(dimethylamino)ethyl]-3-undecylurea was prepared using a similar procedure as was used for the 1-cyclohexyl-3-[2-(dimethylamino)ethyl] urea [48] as follows. Into the ice-cooled stirred solution of 1-isocyanotoundecane (10 g, 35 mmol) in 25 mL of dry acetonitrile, 2.1 g (24 mmol) of 2-(N, N-dimethyl)ethane-1,2-diamine were added dropwise during 15 minutes.…”
Section: Preparation Of 1-[2-(dimethylamino) Ethyl]-3-undecylureamentioning
with the maximum antimicrobial activity found at the spacer length of 6 CH2 groups for bacteria and 8 CH2 groups for fungi. This is related to a different composition of cell membrane of the used microorganisms.
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