Regioselective synthesis of vic-halo alcohols and symmetrical or unsymmetrical vic-dihalides from epoxides using triphenylphosphine-N-halo imides was written by Iranpoor, Nasser;Firouzabadi, Habib;Azadi, Roya;Ebrahimzadeh, Farzaneh. And the article was included in Canadian Journal of Chemistry in 2006.HPLC of Formula: 14070-51-0 This article mentions the following:
A simple, novel, and highly regioselective cleavage of epoxides into vicinal halo alcs. and sym. or unsym. dihalides is described using different stoichiometries of triphenylphosphine and N-halosuccinimide or N-halosaccharine (NXSac). In the experiment, the researchers used many compounds, for example, 2-Chlorobenzo[d]isothiazol-3(2H)-one 1,1-dioxide (cas: 14070-51-0HPLC of Formula: 14070-51-0).
2-Chlorobenzo[d]isothiazol-3(2H)-one 1,1-dioxide (cas: 14070-51-0) belongs to organic chlorides. Organochlorines are organic compounds having multiple chlorine atoms. They were the first synthetic pesticides that were used in agriculture. They are resistant to most microbial and chemical degradations. Alkyl chlorides are versatile building blocks in organic chemistry. While alkyl bromides and iodides are more reactive, alkyl chlorides tend to be less expensive and more readily available.HPLC of Formula: 14070-51-0
Referemce:
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics