117438-63-8

Upstream product

• 629-05-0 n-octyne 
• 1571-08-0 methyl 4-formylbenzoate 

Downstream Products

• 117438-64-9 methyl 4-(1-oxo-2-nonynyl)benzoate 
• 117557-89-8 methyl 4-<1(R)-hydroxy-2-nonynyl>benzoate 
• 117469-78-0 4'-(n-decyloxy)phenyl 4-<(S)-1-((methylsulfonyl)oxy)nonyl>benzoate 
• 113301-59-0 4'-(n-decyloxy)phenyl 4-<1(R)-hydroxy-2-nonynyl>benzoate 
• 117438-59-2 4'-(n-decyloxy)phenyl 4-<(R)-1-fluorononyl>benzoate 
• 113248-18-3 4'-(n-decyloxy)phenyl 4-<(S)-1-hydroxynonynyl>benzoate 
• 117438-65-0 4-<1(R)-hydroxy-2-nonynyl>benzoic acid 

Relevant academic research and scientific papers

Design and synthesis of new ferroelectric liquid crystals. 5.1 properties of some chiral fluorinated FLCs: A direct connection between macroscopic properties and absolute configuration in a fluid phase

In combination with the 'bent cylinder binding site' model for the molecular origins of the ferroelectric polarization P in ferroelectric liquid crystals (FLCs), the observed sign and magnitude of P in mixtures of nonracemic guests with a low-polarization

Chemoselective addition of in situ prepared lithium alkynyl borates to aldehydes: a practical and transition metal free approach toward the synthesis of propargylic alcohols

A convenient synthesis of functionalized propargylic alcohols arising from the 1,2-addition of lithium alkynyl-trimethyl borate onto aldehydes under transition metal free mild conditions is reported. The reaction tolerates a wide range of functional groups, is highly chemoselective and the propargylic alcohols are isolated in good to excellent yields.