84119-04-0

Upstream product

• 84119-02-8 diethyl 2,5-bis(prop-2-yn-1-yloxy)terephthalate 

Downstream Products

• 84119-06-2 2,5-Bis-prop-2-ynyloxy-terephthalic acid didecyl ester 
• 84119-09-5 2,5-Bis-prop-2-ynyloxy-terephthaloyl dichloride 
• 84119-12-0 2,5-Dipropoxy-terephthalic acid didecyl ester 
• 84119-08-4 2,5-Bis-prop-2-ynyloxy-terephthalic acid bis-(2,2-dimethyl-propyl) ester 
• 84119-07-3 2,5-Bis-prop-2-ynyloxy-terephthalic acid diisobutyl ester 
• 84119-14-2 2,5-Dipropoxy-terephthalic acid bis-(2,2-dimethyl-propyl) ester 
• 84119-13-1 2,5-Dipropoxy-terephthalic acid diisobutyl ester 
• 84119-15-3 2,5-Dipropoxy-terephthalic acid dimethyl ester 
• 84119-03-9 2,5-Bis-prop-2-ynyloxy-terephthalic acid dimethyl ester 

Relevant academic research and scientific papers

Passage of Aryl-Tripped Alkyl Groups through Molecular Cavities: The Role of Flexibility

A series of ω-phenylalkyl esters of cyclophane 2 were synthesized.Cyclophane 2 has a cavity ca. 4.5 Angstroem by 6 Angstroem through which the phenylalkyl groups may pass.The activation energy for passage of the phenylalkyl groups through the cyclophane's cavity varies with structure in a manner which suggests dominant importance of alkyl group flexibility.These conclusions are supported by molecular mechanics calculations.