Simple exploration of 707-61-9

As far as I know, this compound(707-61-9)Safety of 4-Methyl-1-phenyl-2,3-dihydro-1H-phosphole 1-oxide can be applied in many ways, which is helpful for the development of experiments. Therefore many people are doing relevant researches.

So far, in addition to halogen atoms, other non-metallic atoms can become part of the aromatic heterocycle, and the target ring system is still aromatic.Alberino, L. M.; Farrissey, W. J.; Sayigh, A. A. R. researched the compound: 4-Methyl-1-phenyl-2,3-dihydro-1H-phosphole 1-oxide( cas:707-61-9 ).Safety of 4-Methyl-1-phenyl-2,3-dihydro-1H-phosphole 1-oxide.They published the article 《Preparation and properties of carbodiimide oligomers》 about this compound( cas:707-61-9 ) in Polymer Preprints (American Chemical Society, Division of Polymer Chemistry). Keywords: carbodiimide oligomer preparation property; phospholene oxide polymerization catalyst; polycarbodiimide oligomer. We’ll tell you more about this compound (cas:707-61-9).

Polycarbodiimides of limited mol. weight were prepared by reacting a difunctional isocyanate, e.g. 4,4′-diisocyanatodiphenylmethane, with a monofunctional isocyanate, e.g. phenyl isocyanate, as terminating agent in the presence of 1-phenyl-3-methyl-2-phospholene-1-oxide [707-61-9] catalyst to give a carbodiimide oligomer [33970-08-0] and CO2. The polymer chains were terminated with end-groups which were equal in thermal stability to the backbone of the polymer. The polymers prepared in the oligomer range having a ratio of equivalents of difunctional to monofunctional isocyanate (r) of 6/1 to 20/1 had mech. properties very nearly equal to those of high mol. weight unterminated polymers. The terminated polymers had a lower melt viscosity than the unterminated polymers and hence a greater ease of processing.

As far as I know, this compound(707-61-9)Safety of 4-Methyl-1-phenyl-2,3-dihydro-1H-phosphole 1-oxide can be applied in many ways, which is helpful for the development of experiments. Therefore many people are doing relevant researches.

Reference:
1,3-Benzodioxole – Wikipedia,
Dioxole | C3H4O2 – PubChem