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Usage

Uses

Used in Pharmaceutical Industry:
E-2-(2,4-Difluorophenyl)vinylboronic acid is used as a reagent in organic synthesis for the preparation of various important organic compounds, including pharmaceuticals. Its unique structure and properties make it a valuable building block in the development of new and diverse pharmaceutical compounds, contributing to the discovery of novel therapeutic agents.
Used in Agrochemical Industry:
E-2-(2,4-Difluorophenyl)vinylboronic acid is also used as a reagent in the synthesis of agrochemicals. Its versatility in organic synthesis allows for the development of new and effective agrochemical compounds, enhancing crop protection and productivity.
Used in Organic Chemistry Research:
As a member of the organoboron compounds class, E-2-(2,4-Difluorophenyl)vinylboronic acid is utilized in various research applications within the field of organic chemistry. Its unique structure and properties make it a valuable tool for exploring new synthetic pathways, developing innovative chemical reactions, and expanding the understanding of organic chemistry principles.

InChI:InChI=1/C14H17BF2O2/c1-13(2)14(3,4)19-15(18-13)8-7-10-5-6-11(16)9-12(10)17/h5-9H,1-4H3/b8-7+

Upstream product

• 73183-34-3 bis(pinacol)diborane 
• 302912-34-1 2,4-difluoroethynylbenzene 
• 288101-48-4 2-(2,4-difluorophenyl)-4,4, 5,5-tetramethyl-1,3,2-dioxaborolane 
• 1105069-27-9 (E)-2-bromovinylboronic acid N-methyliminodiacetic ester 

Relevant academic research and scientific papers

Electrochemical Hydroboration of Alkynes

Herein we reported the electrochemical hydroboration of alkynes by using B2Pin2 as the boron source. This unprecedented reaction manifold was applied to a broad range of alkynes, giving the hydroboration products in good to excellent yields without the need of a metal catalyst or a hydride source. This transformation relied on the possible electrochemical oxidation of an in situ formed borate. This anodic oxidation performed in an undivided cell allowed the formation of a putative boryl radical, which reacted on the alkyne.

Cs4B4O3F10: First Fluorooxoborate with [BF4] Involving Heteroanionic Units and Extremely Low Melting Point

Herein, a new congruently melting mixed-anion compound Cs4B4O3F10 has been characterized as the first fluorooxoborate with [BF4] involving heteroanionic units. Compound Cs4B4O3F10 possesses two highly fluorinated anionic clusters and therefore its formula can be expressed as Cs3(B3O3F6) ? Cs(BF4). The influence of [BF4] units on micro-symmetry and structural evolution was discussed based on the parent compound. More importantly, Cs4B4O3F10 shows the lowest melting point among all the available borates and thus sets a new record for such system. This work is of great significance to enrich and tailor the structure of borates using perfluorinated [BF4] units.

Chemoselective Boronic Ester Synthesis by Controlled Speciation

Control of boronic acid solution speciation is presented as a new strategy for the chemoselective synthesis of boronic esters. Manipulation of the solution equilibria within a cross-coupling milieu enables the formal homologation of aryl and alkenyl boron