653568-72-0

Upstream product

• 653568-68-4 4-methoxymethylbenzothioamide 
• 1515-85-1 4-(methoxymethyl)benzonitrile 
• 653568-70-8 [2-(4-methoxymethyl-phenyl)-thiazol-4-yl]-acetic acid ethyl ester 

Downstream Products

• 653568-74-2 [2-(4-bromomethyl-phenyl)-thiazol-4-yl]-acetic acid 

Relevant academic research and scientific papers

Synthesis of anti-[2.2](2-phenylthiazolophane): A new heterocyclic biphenylophane

Synthesis of a heterocyclic variant of the biphenylophanes, namely anti-[2.2](2-phenylthiazolophane) (1), is described via a sequence involving the pyrolysis of an intermediate bis-lactone (8). Dynamic 1H NMR analysis revealed both the bis-lactone 8 and the target heterophane 1 to be conformationally mobile on the NMR time scale at temperatures down to -55 °C.