111285-12-2

Upstream product

• 110-52-1 1,4-dibromo-butane 
• 623-05-2 (4-hydroxyphenyl)methanol 
• 77355-00-1 1,4-bis(4-formylphenoxy)butane 

Downstream Products

• 163301-70-0 1,4-bis(4-chloromethylphenoxy)butane 
• 1629992-76-2 C₂₄H₂₆O₄ 
• 132939-04-9 3,3'-<1,4-Butanediylbis(oxy-4,1-phenylenemethyleneoxy)>bis<2-(2-propenyloxy)benzaldehyde> 
• 132939-06-1 3,3'-<1,4-Butanediylbis(oxy-4,1-phenylenemethyleneoxy)>bis<2-hydroxybenzaldehyde> 
• 111284-99-2 1,1'-<1,4-Butanediylbis(oxy)>bis<4-(bromomethyl)benzene> 

Relevant academic research and scientific papers

Glaser-Eglinton-Hay sp-sp coupling and macrocyclization: Construction of a new class of polyether macrocycles having a 1,3-diyne unit

Glaser-Eglinton-Hay-type sp-sp coupling, macrocyclization and the construction of skeletally interesting, 18-27 membered, polyether macrocycles having a 1,3-diyne unit-based cylindrical backbone are reported. The utility of polyether macrocycles having th

Analysis and improvement of an anion-templated rotaxane synthesis

A series of new rotaxanes with axles different in length was prepared. Following the synthetic protocol utilizing a known anion template effect (Scheme 1), surprisingly low yields in the order of 2 - 5% were obtained (Scheme 3), which furthermore signific

Bisoxadiazolidine derivative

A bisoxadiazolidine dione derivative represented by the following general formula (I) or a pharmaceutically acceptable salt thereof, which is useful as an insulin sensitivity-increasing drug, and a pharmaceutical composition thereof. STR1 each represents a phenylene group L: (1) an oxygen, (2) a STR2 (3) a --S(O)n --, (4) a --CO--, (5) a STR3 (6) an alkylene group or an alkenylene group which may respectively be interrupted with an oxygen atom and/or a sulfur atom.

Molecular Recognition of Neutral Molecules by Metalloclefts: Synthesis, X-ray Structure, 1H NMR Spectroscopy, Electrochemistry, and Molecular Modeling

Metalloclefts 2 and 10a-b and metallomacrocycles 7a-c possessing a Lewis acidic uranyl cation were synthesized from the corresponding aldehydes.The complexation of these compounds with neutral molecules was assessed by 1H NMR spectroscopy, X-ray structure