Simple exploration of 3229-00-3

This compound(Pentaerythrityltetrabromide)Electric Literature of C5H8Br4 was discussed at the molecular level, the effects of temperature and reaction time on the properties of the compound were discussed, and the optimum reaction conditions were selected.

Banerjee, Rakesh; Maiti, Saikat; Dhara, Dibakar published an article about the compound: Pentaerythrityltetrabromide( cas:3229-00-3,SMILESS:BrCC(CBr)(CBr)CBr ).Electric Literature of C5H8Br4. Aromatic heterocyclic compounds can be classified according to the number of heteroatoms or the size of the ring. The authors also want to convey more information about this compound (cas:3229-00-3) through the article.

In the present work, we have established a novel and environmentally benign method, whereby a 1,3-dipolar cycloaddition reaction was applied using a non-toxic reagent, iodosobenzenediacetate [PhI(OAc)2], instead of the conventional copper-based reagents for the development of star-branched polymers. Here we have demonstrated the synthesis of core cross-linked star (CCS) polymers via the formation of isoxazoline ring using ‘click reaction’ between acrylate functionalities in a polymer chain and in situ generated nitrile oxide groups from a cross-linker added externally. In the initial step, a well-defined styrenic block copolymer with acrylate-functionalized middle-block was synthesized by controlled radical polymerization (RAFT) using α,α’-xylyl-bis(dithiobenzoate) as a chain transfer agent using 4-vinyl benzyl chloride and styrene as comonomers. Thereafter, the chlorobenzyl groups were converted into acrylate by reaction with acrylic acid. In the following step, core cross-linked star (CCS) polymers were synthesized by reacting the above block copolymer and oxime-functionalized cross-linkers (bi- and tetra-functional) using PhI(OAc)2 ‘click chem.’. Formation of CCS polymers was confirmed from NMR, FTIR, GPC and DLS studies.

This compound(Pentaerythrityltetrabromide)Electric Literature of C5H8Br4 was discussed at the molecular level, the effects of temperature and reaction time on the properties of the compound were discussed, and the optimum reaction conditions were selected.

Reference:
Imidazole – Wikipedia,
Imidazole | C3H4N2 – PubChem