118974-47-3

Upstream product

• 118974-46-2 N-[2-(2-hydroxyethoxy)ethyl]acetamide 
• 108-24-7 acetic anhydride 
• 95239-78-4 2-(2-Aminoethoxy)chloroethane 

Downstream Products

• 124243-56-7 N-{2-[2-({2-[2-(2-{[2-(2-Acetylamino-ethoxy)-ethyl]-benzyl-amino}-ethoxy)-ethoxy]-ethyl}-benzyl-amino)-ethoxy]-ethyl}-acetamide 
• 124266-42-8 N-[2-(2-{Benzyl-[2-(2-benzylamino-ethoxy)-ethyl]-amino}-ethoxy)-ethyl]-acetamide 
• 124243-55-6 N-[2-(2-{[2-(2-{[2-(2-Acetylamino-ethoxy)-ethyl]-benzyl-amino}-ethoxy)-ethyl]-benzyl-amino}-ethoxy)-ethyl]-acetamide 
• 118974-48-4 N-[2-(2-{[2-(2-Acetylamino-ethoxy)-ethyl]-benzyl-amino}-ethoxy)-ethyl]-acetamide 
• 128620-78-0 10-Benzyl-16-ethyl-1,4,7,13-tetraoxa-10,16-diaza-cyclooctadecane 
• 128620-69-9 7-Benzyl-13-ethyl-1,4,10-trioxa-7,13-diaza-cyclopentadecane 
• 128620-59-7 [2-(2-Benzylamino-ethoxy)-ethyl]-ethyl-amine 
• 124243-46-5 Benzyl-[2-(2-benzylamino-ethoxy)-ethyl]-[2-(2-ethylamino-ethoxy)-ethyl]-amine 
• 118974-41-7 23-<(allyloxy)methyl>-4,13-dibenzyl-19,28-diethyl-4,13,19,28-tetraza-1,7,10,16,22,25-hexaoxacyclotriacontane 
• 118974-40-6 20-<(allyloxy)methyl>-4,10-dibenzyl-16,25-diethyl-4,10,16,25-tetraza-1,7,13,19,22-pentaoxacycloheptacosane 
• 118974-45-1 {2-[2-(Benzyl-{2-[2-(2-{benzyl-[2-(2-ethylamino-ethoxy)-ethyl]-amino}-ethoxy)-ethoxy]-ethyl}-amino)-ethoxy]-ethyl}-ethyl-amine 
• 119004-92-1 [2-(2-{Benzyl-[2-(2-{benzyl-[2-(2-ethylamino-ethoxy)-ethyl]-amino}-ethoxy)-ethyl]-amino}-ethoxy)-ethyl]-ethyl-amine 
• 118974-37-1 4-<(allyloxy)methyl>-4-benzyl-10,19-diethyl-4,10,19-triaza-1,7,13,16-tetraoxycycloheneicosane 
• 118974-49-5 10-Benzyl-4,16-diethyl-1,7,13-trioxa-4,10,16-triaza-cyclooctadecane-3,17-dione 

Relevant academic research and scientific papers

Synthesis and in vitro antitumor activity of novel 2-alkyl-5- methoxycarbonyl-11-methyl-6H-pyrido[4,3-b]carbazol-2-ium and 2-alkylellipticin-2-ium chloride derivatives

Twenty-one types of novel ellipticine derivatives and pyridocarbazoles (5-methoxycarbonyl-11-methyl-6H-pyrido[4,3-b]carbazoles) with a nitrosourea moiety, linked by an oxydiethylene unit at the 2 position, were synthesized, and their cytotoxicity against HeLa S-3 cells was evaluated. Some of these new compounds exhibited potent antitumor activity by comparison with that of ellipticine.

A New Building Block Method to Synthesize Symmetrical and Asymmetrical Per-N-alkyl-Substituted Polyaza-Crown Compounds

A new approach for the synthesis of a variety of per-N-alkylated polyaza-crown compounds is decscribed.N-acetamide (25) and its benzamide analogue 26 are the key building blocks for the synthesis of the new polyaza-crowns.These ch

NOVEL AND CONVENIENT SYNTHESES OF N-ALKYL-SUBSTITUTED TRIAZA- AND TETRAAZA-CROWN COMPOUNDS

A new short method to prepare N-alkyl-substituted triaza- and tetraaza-crown compounds in good overall yield by reacting the appropriate oligoazaoxadiamine with allyloxymethyl-substituted triethylene glycol diiodide or diglycolyl dichloride (followed by r