5565-36-6

Usage

Uses

Used in Organic Synthesis:
1,4-Benzenediboronic acid bis(neopentyl glycol) ester is used as a reagent in Suzuki-Miyaura cross-coupling reactions for the formation of carbon-carbon bonds. Its application facilitates the synthesis of various organic compounds, contributing to the development of new chemical entities.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 1,4-Benzenediboronic acid bis(neopentyl glycol) ester is used as a building block for the preparation of complex organic molecules. Its unique reactivity allows for the creation of novel drug candidates with potential therapeutic applications.
Used in Agrochemical Industry:
Similarly, in the agrochemical industry, 1,4-Benzenediboronic acid bis(neopentyl glycol) ester is utilized as a precursor in the synthesis of agrochemicals, such as pesticides and herbicides, to develop more effective and environmentally friendly products.
Used in Organic Material Synthesis:
1,4-Benzenediboronic acid bis(neopentyl glycol) ester is also employed in the synthesis of organic materials, including polymers and advanced materials, for various applications in fields such as electronics, materials science, and nanotechnology. Its versatility in forming complex structures makes it an essential component in the development of innovative materials.

InChI:InChI=1/C16H24B2O4/c1-15(2)9-19-17(20-10-15)13-5-7-14(8-6-13)18-21-11-16(3,4)12-22-18/h5-8H,9-12H2,1-4H3

Upstream product

• 4612-26-4 1,4-Phenyldiboronic acid 
• 126-30-7 2,2-Dimethyl-1,3-propanediol 
• 214360-44-8 2-(4-cyanophenyl)-5,5-dimethyl[1,3,2]dioxaborinane 
• 201733-56-4 2-(5,5-dimethyl-1,3,2-dioxaborinan-2-yl)-5,5-dimethyl-1,3,2-dioxaborinane 
• 106-46-7 para-dichlorobenzene 
• 668987-38-0 5,5-dimethyl-1,3,2-dioxaborinane 
• 71-43-2 benzene 
• 688-74-4 boric acid tributyl ester 
• 106-37-6 1.4-dibromobenzene 
• 121-43-7 Trimethyl borate 

Downstream Products

• 1116113-75-7 4,4''''-di-(1-pentylnonyl)-p-quinquephenyl 
• 113268-53-4 p-Trifluorovinyl α,β,β-trifluorostyrene 
• 1417418-28-0 C₁₄H₁₄I⁽¹⁺⁾*C₂F₃O₂^(1-) 
• 1417418-13-3 (4-(5,5-dimethyl-1,3,2-dioxaborinan-2-yl)phenyl)(phenyl)iodonium trifluoroacetate 
• 1417418-12-2 (4-(5,5-dimethyl-1,3,2-dioxaborinan-2-yl)phenyl)(phenyl)iodonium tosylate 
• 1006603-40-2 C₈₆H₁₁₀O₈ 

Relevant academic research and scientific papers

Anionic Conjugated Polyelectrolytes for FRET-based Imaging of Cellular Membrane Potential

We report a F?rster resonance energy transfer (FRET)-based imaging ensemble for the visualization of membrane potential in living cells. A water-soluble poly(fluorene-cophenylene) conjugated polyelectrolyte (FsPFc10) serves as a FRET donor to a voltage-sensitive dye acceptor (FluoVolt?). We observe FRET between FsPFc10 and FluoVolt?, where the enhancement in FRET-sensitized emission from FluoVolt? is measured at various donor/acceptor ratios. At a donor/acceptor ratio of 1, the excitation of FluoVolt? in a FRET configuration results in a three-fold enhancement in its fluorescence emission (compared to when it is excited directly). FsPFc10 efficiently labels the plasma membrane of HEK 293T/17 cells and remains resident with minimal cellular internalization for ~ 1.5 h. The successful plasma membrane-associated colabeling of the cells with the FsPFc10-FluoVolt? donor-acceptor pair is confirmed by dual-channel confocal imaging. Importantly, cells labeled with FsPFc10 show excellent cellular viability with no adverse effect on cell membrane depolarization. During depolarization of membrane potential, HEK 293T/17 cells labeled with the donor-acceptor FRET pair exhibit a greater fluorescence response in FluoVolt? emission relative to when FluoVolt? is used as the sole imaging probe. These results demonstrate the conjugated polyelectrolyte to be a new class of membrane labeling fluorophore for use in voltage sensing schemes.

Zinc(II) and Copper(II) Metal–Organic Frameworks Constructed from a Terphenyl-4,4′′-dicarboxylic Acid Derivative: Synthesis, Structure, and Catalytic Application in the Cyanosilylation of Aldehydes

Solvothermal reaction of zinc(II) and copper(II) salts with 3,3′′-dipropoxy-[1,1′:4′,1′′-terphenyl]-4,4′′-dicarboxylic acid (H2L) gave rise to the 1D and 2D metal–organic frameworks (MOFs) [Zn(L)(dmf)2]n(1), [Zn2/sub

Rhodium(I)-catalyzed borylation of nitriles through the cleavage of carbon-cyano bonds

The reaction of aryl cyanides with diboron in the presence of a rhodium/Xantphos catalyst and DABCO affords arylboronic esters via carbon-cyano bond cleavage. This unprecedented mode of reactivity for a borylrhodium species allows the regioselective intro

CARBON NANORING, METHOD FOR PRODUCING SAME, COMPOUND SUITABLE AS STARTING MATERIAL FOR PRODUCING THE CARBON NANORING, AND METHOD FOR PRODUCING THE COMPOUND

This invention provides: a compound for accurately forming a carbon nanoring that contains a specific number of organic rings and has a definite diameter; a method for producing the compound; a method for efficiently producing a carbon nanoring; and a cyc

Synthesis, optical, and electronic properties of soluble poly-p-phenylene oligomers as models for molecular wires

A homologous series of soluble poly-p-phenylenes containing up to eight phenylene moieties(pp2-pp8)with branched iso-alkyl(or bis-n-alkylmethyl)groups has been synthesized and the structure-property relationship with regards to various optical and electronic properties established. All electronic and optoelectronic properties of poly-p-phenylenes followed a 1/n relationship(where n is number of phenylene moieties)with the increasing number of phenylene moieties. The low-energy electronic transition of the pp2-PP7 cation radicals, generated either by laser-flash photolysis or by chemical oxidation,varied as well according to the inverse(1/n)relationship. The observed inverse relationship of all measured electronic and optoelectronic prope rties against the increasing number of phenylene units in various ppn's, as well as X-ray crystallography of both neutral and a cation-radical salt of a representative tetra-p-phenylene oligomer allows us to demonstrate that the effective conjugation length in poly-p-phenylenes is, in part, controlled by the increasing number of interactions of ortho hydrogens which may prevent simultaneous planarization of the continuous arrays of a large number of phenylene moieties.

Neopentylglycolborylation of aryl chlorides catalyzed by the mixed ligand system NiCl2(dppp)/dppf

The mixed ligand system 10 mol % NICl2(dppp) with 5 mol % dppf was discovered to be an extremely efficient catalyst for the neopentylglycolborylation of a diversity of electron-rich and electron-deficient aryl chlorides. Optimization showed tha