Gao, Xingming et al. published their research in Bioorganic & Medicinal Chemistry Letters in 2015 | CAS: 166821-88-1

2-(2-(Bromomethyl)phenyl)-5,5-dimethyl-1,3,2-dioxaborinane (cas: 166821-88-1) belongs to organobromine compounds. Bromo compounds are employed in a variety of metal-catalyzed coupling reactions. They are also ideal candidates for the synthesis of Grignard reagents that have wide-applicability in organic synthesis. alpha-Bromoesters are employed in the Reformatsky reaction for the synthesis of beta-hydroxyesters. When the molecular ion is detected, the bromine and chlorine isotope patterns are very distinct, but caution is to be exercised for certain mixed chlorinated/brominated compounds, which can look similar to homohalogen patterns.SDS of cas: 166821-88-1

A fluorescent bisboronic acid compound that selectively labels cells expressing oligosaccharide Lewis X was written by Gao, Xingming;Zhu, Mengyuan;Fan, Haiying;Yang, Wenqian;Ni, Weijuan;Karnati, Vishnu V. R.;Gao, Shouhai;Carson, John;Weston, Brent;Wang, Binghe. And the article was included in Bioorganic & Medicinal Chemistry Letters in 2015.SDS of cas: 166821-88-1 This article mentions the following:

Two fluorescent diboronic acid compounds with a dipeptide linker were synthesized as potential sensors for cell surface saccharide Lewis X (LeX). Compound 6a (I) with a dipeptide (H-Asp-Ala-) as the linker was found to selectively label CHOFUT4 cells, which express Lex, at micromolar concentrations, while non-Lex-expressing control cells were not labeled. In the experiment, the researchers used many compounds, for example, 2-(2-(Bromomethyl)phenyl)-5,5-dimethyl-1,3,2-dioxaborinane (cas: 166821-88-1SDS of cas: 166821-88-1).

2-(2-(Bromomethyl)phenyl)-5,5-dimethyl-1,3,2-dioxaborinane (cas: 166821-88-1) belongs to organobromine compounds. Bromo compounds are employed in a variety of metal-catalyzed coupling reactions. They are also ideal candidates for the synthesis of Grignard reagents that have wide-applicability in organic synthesis. alpha-Bromoesters are employed in the Reformatsky reaction for the synthesis of beta-hydroxyesters. When the molecular ion is detected, the bromine and chlorine isotope patterns are very distinct, but caution is to be exercised for certain mixed chlorinated/brominated compounds, which can look similar to homohalogen patterns.SDS of cas: 166821-88-1

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary