145708-71-0

Upstream product

• 132170-05-9 2,5-Bis(trimethylsilyl)bicyclo<4.2.0>octa-1,3,5-triene 
• 694-87-1 benzocyclobutene 

Downstream Products

• 1359869-55-8 C₁₈H₁₆O₂ 
• 1359869-56-9 C₁₈H₁₄Br₂O₂ 
• 1359869-57-0 C₄₀H₅₀N₂O₁₀ 
• 145708-75-4 1,2-dihydro-N,N'-diphenylcyclobutabenzene-3,6-dicarboxamide 

Relevant academic research and scientific papers

High temperature thermosets derived from benzocyclobutene-containing main-chain oligomeric carbosilanes

A series of benzocyclobutene-carbosilane thermosets derived from benzocyclobutene-containing oligomeric silylenephenylene (PBSEPs) were synthesized. DSC analysis results demonstrated that the reaction of PBSEPs presumably took place within the temperature

COMPOUNDS AS HEPATITIS C VIRUS INHIBITORS AND PHARMACEUTICAL USES THEREOF

The invention provides compounds as hepatitis C virus inhibitors and pharmaceutical uses thereof. Specifically, the invention provides compounds of Formula (I) or a stereoisomer, a tautomer, an enantiomer, an N-oxide, a hydrate, a solvate, a metabolite, a

HEPATITIS C VIRUS INHIBITORS

The present disclosure relates to compounds, compositions and methods for the treatment of hepatitis C virus (HCV) infection. Also disclosed are pharmaceutical compositions containing such compounds and methods for using these compounds in the treatment o

GAMMA SECRETASE MODULATORS

This invention provides novel compounds that are modulators of gamma secretase. The compounds have the formula (I). Also disclosed are methods of modulating gamma secretase activity and methods of treating Alzheimer's Disease using the compounds of formula (I).

Cyclobutabenzene monomers

Novel difunctionalized cyclobutabenzene monomers of the general formula: STR1 wherein Z can be hydrogens or a cyclobutane ting; and X and Y are carbox amino, alcohol, isocyanate, acid halide, or bis-acyl fluoride groups. In a particularly preferred embodiment, the cyclobutabenzene derivative is 1,2-dihydrocyclobutabenzene-3,6-carboxylic acid. The difunctionalized cyclobutabenzene monomer can form part of a polymer backbone chain, but has an additional functionality, the butane ring, which can be easily opened to produce strong, covalent bond crosslinking between polymer chains. The crosslinking can be induced simply by heating the polymer to a temperature in excess of 300° C.

A high-yield route to 1,2-dihydrocyclobutazene-3,6-dicarboxylic acid

A simple five-step method for preparing the previously unknown 1.2-dihydrocyclobutabenzene-3,6-dicarboxylic acid (XTA) in high yield is presented. All intermediates were crystalline compounds which allowed the preparation to be scaled up without complication. The title compound is of interest as a crosslinkable derivative of the widely used monomer, terephthalic acid (TA).