154786-34-2

Upstream product

• 629-11-8 1,6-hexanediol 
• 134-96-3 syringic aldehyde 
• 2009-83-8 6-chloro-1-hexanol 
• 4286-55-9 1-bromo-6-hexanol 

Downstream Products

• 1425539-66-7 (2Z)-2-(1,3-benzodioxol-5-yl)-3-{4-[(6-hydroxyhexyl)oxy]-3,5-dimethoxyphenyl}prop-2-enenitrile 
• 1425539-63-4 (2Z)-2-(3,4-dimethoxyphenyl)-3-{4-[(6-hydroxyhexyl)oxy]-3,5-dimethoxyphenyl}prop-2-enenitrile 
• 1425539-64-5 6-{4-[(Z)-2-cyano-2-(3,4-dimethoxyphenyl)ethenyl]-2,6-dimethoxyphenoxy}hexyl 2-methylacrylate 
• 1425539-67-8 6-{4-[(Z)-2-(1,3-benzodioxol-5-yl)-2-cyanoethenyl]-2,6-dimethoxyphenoxy}hexyl 2-methylacrylate 
• 864161-32-0 4-[6-(4-formylphenoxy)hexoxy]-3,5-dimethoxybenzaldehyde 

Relevant academic research and scientific papers

Stilbenophane analogues of deoxycombretastatin A-4

A new family of polyoxygenated stilbenophanes has been synthesized as conformationally restricted analogues of antimitotic combretastatins. By means of the McMurry olefination process, compounds derived from diethyleneglycol and 1,6-hexanediol were obtain

Photoreactive compounds

The present invention relates to photoreactive compounds that are particularly useful in materials for the alignment of liquid crystals.

PHOTOREACTIVE COMPOUNDS

The present invention relates to photoreactive compounds that are particularly useful in materials for the alignment of liquid crystals.

Synthesis and conformational analysis of macrocyclic dihydroxystilbenes linked between the para-para positions

A new family of diphenylethanes has been synthesized as conformationally restricted analogues of antimitotic combretastatins. The two phenyl rings are linked between the para-phenolic positions through a 3-oxapentamethylene or hexamethylene chain. The key

Bifunctional [c2]daisy-chains and their incorporation into mechanically interlocked polymers

A strategy for the formation of mechanically interlocked polymers is presented. Ring-closing olefin metathesis has been shown to provide a very high yielding route to [c2]daisy-chains suitably functionalized to allow their one-step conversion to bisolefin