Vermeij, Rudolf J. et al. published their research in Australian Journal of Chemistry in 2010 | CAS: 313648-56-5

Dimethyl 5-ethynylisophthalate (cas: 313648-56-5) belongs to esters. Esters are widespread in nature and are widely used in industry. In nature, fats are in general triesters derived from glycerol and fatty acids. Esters are responsible for the aroma of many fruits. Liquid esters of low volatility serve as softening agents for resins and plastics. Esters also include many industrially important polymers. Polymethyl methacrylate is a glass substitute sold under the names Lucite and Plexiglas; polyethylene terephthalate is used as a film (Mylar) and as textile fibres sold as Terylene, Fortrel, and Dacron.Safety of Dimethyl 5-ethynylisophthalate

Mixed [2.2]Cyclophanes of Pyrene and Benzene was written by Vermeij, Rudolf J.;Miller, David O.;Dawe, Louise N.;Aprahamian, Ivan;Sheradsky, Tuvia;Rabinovitz, Mordecai;Bodwell, Graham J.. And the article was included in Australian Journal of Chemistry in 2010.Safety of Dimethyl 5-ethynylisophthalate This article mentions the following:

An examination of the literature on [2.2]cyclophanes reveals a loose relationship between the relative sizes of the two half-cyclophanes’ (as measured by the parameter Δd) and the limitations of the dominant general synthetic approaches. Direct coupling methods tend to be successful only for systems with Δd values below 1.0Å, whereas ring-contraction-based approaches are usually viable for systems with Δd values up to 2.0 Å. For the very few known systems with Δd values greater than 2.0 Å, aromatization-based approaches are the only ones that have been successful. The syntheses of two [2.2]cyclophanes with very large Δd values, [2]para-cyclo[2](2,7)pyrenophane (17) (Δd=4.25 Å) and [2]meta-cyclo[2](2,7)pyrenophane (18) (Δd=5.04 Å) are presented here. The syntheses hinge on a valence isomerization/dehydrogenation reaction. The crystallog. determined bend angle, θ, for 18 is 96.1°. Cyclophane 18 undergoes a degenerate conformational flip, the energy barrier for which was determined to be 18.9 kcalmol-1 by DNMR. In the experiment, the researchers used many compounds, for example, Dimethyl 5-ethynylisophthalate (cas: 313648-56-5Safety of Dimethyl 5-ethynylisophthalate).

Dimethyl 5-ethynylisophthalate (cas: 313648-56-5) belongs to esters. Esters are widespread in nature and are widely used in industry. In nature, fats are in general triesters derived from glycerol and fatty acids. Esters are responsible for the aroma of many fruits. Liquid esters of low volatility serve as softening agents for resins and plastics. Esters also include many industrially important polymers. Polymethyl methacrylate is a glass substitute sold under the names Lucite and Plexiglas; polyethylene terephthalate is used as a film (Mylar) and as textile fibres sold as Terylene, Fortrel, and Dacron.Safety of Dimethyl 5-ethynylisophthalate

Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics