40447-21-0Relevant academic research and scientific papers
Triazolo[4,5-f]quinolines. Part VI. Synthesis and evaluation of 9-aminoalkyl(aryl)-2-methyl-2H-[4,5-f]quinolines as anticancer agents. Preliminary results of in vitro screening
Sanna,Sequi,Pagletti
, p. 47 - 54 (2007/10/02)
9-Aminoalkyl(aryl)-2-methyl-2H-triazolo[4,5-f]quinolines were prepared in order to evaluate their in vitro antitumor activity. Some members of this series exbibited both cell selectivity and tumor growth inhibition activity at concentrations between 10su
Quaternary alkynoxymethyl amines
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, (2008/06/13)
This invention relates to quaternaries of alkynoxymethyl amines and uses thereof. These may be summarized by the following formulae: STR1 where R and R' are substituted groups such as alkyl, aryl, etc.; R'" is an acetylenic group; and X is an anion; and STR2 where R and R'" having the same meaning as in (1) and Z is a bridging group, preferably hydrocarbon such as alkylene, alkinylene, alkenylene, arylene, etc.
Microbiocidal quaternaries of halogen derivatives of alkynoxymethyl amines
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, (2008/06/13)
This invention relates to quaternaries of halogen derivatives of alkynoxymethyl amines and uses thereof. These may be summarized by the following formulae: STR1 where R and R' are substituted groups such as alkyl, aryl, etc.; R" is an alkylidene group; and X is halogen and A is an anion; and STR2 where R, R' and R" having the same meaning as in (1) and Z is a bridging group, preferably hydrocarbon such as alkylene, alkinylene, alkenylene, arylene, etc.
Halogen derivatives of alkynoxymethyl amines
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, (2008/06/13)
This invention relates to halogen derivatives of alkynoxymethylamines and to uses thereof. The present invention may be ideally illustrated by the following equation: where R is a substituted group, preferably hydrocarbon, such as alkyl, cycloalkyl, aryl, etc., R' is hydrocarbon, preferably alkylene, and where X is halogen.
Alkynoxymethyl amines
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, (2008/06/13)
This invention relates to alkynoxymethyl amines, to methods of preparing them, and uses thereof, particularly as corrosion inhibitors. These compounds are prepared by reacting an amine, such as RNH2, with an aldehyde, such as formaldehyde, and an alkynol, such as propargyl alcohol, to yield compounds of the formula where R is a substituted group, preferably alkyl, cycloalkyl, aryl, etc., and R' is an acetylenic alcohol moiety.
