Molinaro, Carmela et al. published their research in Journal of Organic Chemistry in 2019 | CAS: 68716-49-4

2-(4-Bromophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane (cas: 68716-49-4) belongs to alcohols. Alcohols are among the most common organic compounds. They are used as sweeteners and in making perfumes, are valuable intermediates in the synthesis of other compounds, and are among the most abundantly produced organic chemicals in industry. Tertiary alcohols cannot be oxidized at all without breaking carbon-carbon bonds, whereas primary alcohols can be oxidized to aldehydes or further oxidized to carboxylic acids.Formula: C12H16BBrO2

Synthesis of a CGRP Receptor Antagonist via an Asymmetric Synthesis of 3-Fluoro-4-aminopiperidine was written by Molinaro, Carmela;Phillips, Eric M.;Xiang, Bangping;Milczek, Erika;Shevlin, Michael;Balsells, Jaume;Ceglia, Scott;Chen, Jiahui;Chen, Lu;Chen, Qinghao;Fei, Zhongbo;Hoerrner, Scott;Qi, Ji;de Lera Ruiz, Manuel;Tan, Lushi;Wan, Baoqiang;Yin, Jingjun. And the article was included in Journal of Organic Chemistry in 2019.Formula: C12H16BBrO2 This article mentions the following:

A practical and efficient enantioselective synthesis of the calcitonin gene-related peptide receptor antagonist I has been developed. The key structural component of the active pharmaceutical ingredient is a syn-1,2-amino-fluoropiperidine II•2HCl. Two approaches were developed to synthesize this important pharmacophore. Initially, Ru-catalyzed asym. hydrogenation of fluoride-substituted enamide III enabled the synthesis of sufficient quantities of compound I to support early preclin. studies. Subsequently, cost-effective route to this intermediate was developed utilizing a dynamic kinetic asym. transamination of tert-Bu 3-fluoro-4-oxopiperidine-1-carboxylate. This synthesis also features a robust Ullmann coupling to install a bis-aryl ether using a soluble Cu(I) catalyst. Finally, an enzymic desymmetrization of meso-dimethyl 3-methylglutarate was exploited for the construction of the γ-lactam moiety in I. In the experiment, the researchers used many compounds, for example, 2-(4-Bromophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane (cas: 68716-49-4Formula: C12H16BBrO2).

2-(4-Bromophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane (cas: 68716-49-4) belongs to alcohols. Alcohols are among the most common organic compounds. They are used as sweeteners and in making perfumes, are valuable intermediates in the synthesis of other compounds, and are among the most abundantly produced organic chemicals in industry. Tertiary alcohols cannot be oxidized at all without breaking carbon-carbon bonds, whereas primary alcohols can be oxidized to aldehydes or further oxidized to carboxylic acids.Formula: C12H16BBrO2

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts