242487-95-2

Upstream product

• 242487-86-1 1,5-bis(4-N,N-dimethylaminophenyl)-1,4-pentadiyn-3-ol 
• 242487-90-7 1,5-bis(4-N,N-dimethylaminophenyl)-1,4-pentadiyn-3-one 
• 17573-94-3 4-ethynyl-N,N-dimethylaniline 
• 586-77-6 4-bromo-N,N-dimethylaniline 
• 40230-97-5 N,N-dimethyl-4-[(trimethylsilyl)ethynyl]aniline 
• 242488-03-5 (Z)-1,5-Bis-(4-dimethylamino-phenyl)-1-ethoxy-pent-1-en-4-yn-3-one 

Relevant academic research and scientific papers

2,4,6-triarylchalcogenopyrylium dyes related in structure to the antitumor agent AA1 as in vitro sensitizers for the photodynamic therapy of cancer

Cationic chalcogenopyrylium dyes 2-4 were synthesized in six steps from 4-(dimethylamino)phenylethyne (7), have absorption maxima in methanol of 594, 631, and 672 nm, respectively, and generate singlet oxygen with quantum yields [Φ(1O2/su

Chalcogenopyranones from disodium chalcogenide additions to 1,4- pentadiyn-3-ones. The role of enol ethers as intermediates

Enol ethers 9 are formed as a mixture of E- and Z-isomers from the addition of ethanol to 1,4-pentadiyn-3-ones 2 in sodium ethoxide/ethanol. The enol ethers react with disodium chalcogenides to give the corresponding 2,6- disubstituted chalcogenopyranones