scholarly journals [(3-Chlorobenzamido)methyl]triethylammonium Chloride

Molbank ◽  
10.3390/m851 ◽  
2015 ◽  
Vol 2015 (2) ◽  
pp. M851
Author(s):  
Pranvera Breznica-Selmani ◽  
Kristina Mladenovska ◽  
Zoran Kavrakovski ◽  
Bozhana Mikhova ◽  
Gerald Draeger ◽  
...  
Keyword(s):  
Triethylammonium Chloride

(Chloromethyl)triethylammonium chloride monohydrate

2006 ◽  
Vol 62 (7) ◽  
pp. o2836-o2837 ◽  
Author(s):  
Monika Haberecht ◽  
Hans-Wolfram Lerner ◽  
Michael Bolte
Keyword(s):  
Hydrogen Bonds ◽  
Title Compound ◽  
Water Molecules ◽  
Compound C ◽  
Chloride Monohydrate ◽  
Triethylammonium Chloride

The title compound, C7H17ClN+·Cl−·H2O, is composed of discrete (chloromethyl)triethylammonium cations, Cl− anions and water molecules, which are held together by O—H...Cl hydrogen bonds.

Antimicrobial Activity of Triethylammonium Chloride-N-Substituted N′-Cyano-O-(triphenylstannyl)-isourea Complexes

1984 ◽  
Vol 73 (7) ◽  
pp. 1012-1013 ◽  
Author(s):  
Eugene J. Kupchik ◽  
Michael A. Pisano ◽  
Dilipkumar K. Parikh ◽  
Carolyn Krejci ◽  
Jonathan Taylor
Keyword(s):  
Antimicrobial Activity ◽  
Triethylammonium Chloride

Micellar catalysis of the basic hydrolysis of N-methyl-N-(4'-nitropheny1)-2-phenoxyacetamide. Variation of the magnitude of catalysis for differentsources of hydroxide ions

1981 ◽  
Vol 34 (8) ◽  
pp. 1615 ◽  
Author(s):  
TJ Broxton
Keyword(s):  
Sodium Hydroxide ◽  
Cetyltrimethylammonium Bromide ◽  
Reaction System ◽  
Micellar Catalysis ◽  
Buffer System ◽  
Nucleophilic Catalysis ◽  
Carbonate Ions ◽  
Basic Hydrolysis ◽  
Hydrolysis Of ◽  
Triethylammonium Chloride

The hydrolysis of N-methyl-N-(4'-nitrophenyl)-2-phenoxyacetamide has been studied in the presence and absence of micelles of cetyltrimethylammonium bromide. The micellar catalysis depends on the reaction system being used. Hydrolysis in the presence of sodium hydroxide, and in the presence of borate, carbonate/bicarbonate and triethylamine/triethylammonium chloride buffers has been examined. The magnitude of catalysis is shown to depend on the buffer system used, the concentration of detergent, the concentration of the buffer, the pH and the presence of any added salts. The results confirm that it is unrealistic to compare independent sets of results on different compounds unless the conditions for obtaining those results are identical. ��� Hydrolysis in the presence of carbonate/bicarbonate buffers is shown to be subject to buffer catalysis and, by analogy with results for p-nitrophenyl acetate, nucleophilic catalysis by carbonate ions is suggested.

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