The compound “1,3,5,2,4,6-Trioxatriborinane” corresponds to an alternative name for boroxine (B3H3O3), which is also known as cyclic trimer of boric acid. The systematic name for boroxine is “1,3,5-Trioxane-2,4,6-trione.”

As the name suggests, it is a cyclic compound consisting of three boron atoms and three oxygen atoms arranged in a ring structure. The chemical formula B3H3O3 represents the molecular composition, with three boron atoms (B), three hydrogen atoms (H), and three oxygen atoms (O).

Boroxine has a unique six-membered ring structure with alternating boron and oxygen atoms. Each boron atom is bonded to one oxygen atom and two hydrogen atoms in the ring. The molecule has a planar geometry, and it is a highly reactive compound.

Boroxine and its derivatives have been studied for various applications in coordination chemistry, catalysis, and materials science. However, its reactivity and difficulty in handling limit its practical uses. As with any boron-containing compound, it is essential to handle boroxine with care and observe appropriate safety measures due to its potential hazards.