609848-03-5

Upstream product

• 119227-71-3 9-decynyl mesylate 
• 220641-23-6 1-O-(triphenylmethyl)-3-O-(4'-methoxybenzyl)-sn-glycerol 
• 482620-96-2 1-((S)-2-Dec-9-ynyloxy-3-trityloxy-propoxymethyl)-4-methoxy-benzene 

Downstream Products

• 609848-15-9 C₈₄H₁₀₄O₆ 
• 609848-13-7 C₈₄H₁₀₆O₆ 
• 486403-08-1 C₆₂H₉₂O₈ 
• 609848-05-7 C₆₂H₉₄O₈ 
• 609848-11-5 (S)-2-[20-((S)-1-Hydroxymethyl-2-trityloxy-ethoxy)-icosa-9,11-diynyloxy]-3-trityloxy-propan-1-ol 
• 609848-04-6 (R)-2-{20-[(R)-1-Hydroxymethyl-2-(4-methoxy-benzyloxy)-ethoxy]-icosa-9,11-diynyloxy}-3-(4-methoxy-benzyloxy)-propan-1-ol 

Relevant academic research and scientific papers

Design, synthesis, and self-assembly of an ether and amide linkage-based cyclic lipid

A novel 48-membered cyclic lipid, in which two ether and two amide groups serve as a linker between its hydrophilic and hydrophobic moiety, was synthesized starting from d-1,2-O-isopropylidene-sn-glycerol. The synthetic scheme is featured by the selective

Efficient synthesis of parallel cyclobolaphiles having two diacetylenes: Mimetics of archaeal membrane lipids

Chiral 48-membered parallel cyclobolaphiles and their diastereomer having two diacetylenes were efficiently synthesized by utilizing both the selective deprotection and the cross-coupling method of two distinct acetylenic compounds.