1301742-87-9

Upstream product

• 1301742-86-8 2-[2-(2-bromophenyl)ethynyl]benzaldehyde 
• 1066-54-2 trimethylsilylacetylene 
• 766-46-1 2-bromo-1-ethynylbenzene 
• 26260-02-6 2-iodobenzaldehyde 
• 38846-64-9 2-ethynylbenzaldehyde 
• 583-55-1 1-Bromo-2-iodobenzene 

Downstream Products

• 1301743-20-3 C₇₈H₅₆N₂ 
• 1301742-88-0 2-(2-ethynylphenylethynyl)benzaldehyde 
• 1301742-98-2 C₆₂H₃₈N₂ 
• 1301743-17-8 C₆₄H₄₄N₂ 
• 1048972-22-0 1-ethynyl-2-((2-vinylphenyl)ethynyl)benzene 

Relevant academic research and scientific papers

Systematic investigation of silver-carbon bonding in coordination frameworks with aryl ligands that contain ethynyl and ethenyl substituents

Single-crystal X-ray diffraction of a series of ten crystalline silver(I)-trifluoroacetate complexes that contained designed ligands, each of which was composed of an aromatic system that was functionalized with terminal and internal ethynyl groups and a

Enantioselective sensing of amines based on [1 + 1]-, [2 + 2]-, and [1 + 2]-condensation with fluxional arylacetylene-derived dialdehydes

Four induced circular dichroism (ICD) probes exhibiting a stereodynamic arylacetylene framework and terminal aldehyde units have been prepared. The CD silent sensors generate a strong chiroptical response to substrate-controlled induction of axial chirality upon selective [1 + 1]-, [2 + 2]-, and [1 + 2]-condensation. The intense Cotton effects can be exploited for in situ ICD analysis of the absolute configuration and ee of a wide range of amines.