57863-69-1

Usage

Uses

Used in Polymer Synthesis:
5-Bromoisophthaloyl dichloride is used as a reactive intermediate for the synthesis of high-performance polymers. Its role is crucial in the production of liquid crystal polymers and polyimides, which are known for their exceptional properties and are used in a variety of applications due to their strength and stability.
Used in Advanced Material Production:
In the industry of advanced materials, 5-Bromoisophthaloyl dichloride is utilized as a crosslinking agent. This application enhances the mechanical and thermal properties of the materials, leading to the development of products with improved performance characteristics suitable for specialized applications.
Used in the Chemical Industry:
5-Bromoisophthaloyl dichloride is also employed in the chemical industry for the creation of various compounds and materials that require its specific reactivity and bonding capabilities. Its versatility makes it a valuable component in a wide range of chemical processes and formulations.

Upstream product

• 23351-91-9 5-bromoisophthalic acid 
• 51760-21-5 dimethyl 5-bromoisophthalate 

Downstream Products

• 160892-06-8 5-bromo-1,3-benzenedicarboxamide 
• 160892-07-9 5-bromo-1,3-benzenedicarbonitrile 
• 160892-05-7 2,2'-(5-bromo-1,3-phenylene)bisimidazole 
• 160892-04-6 2,2'-(5-bromo-1,3-phenylene)bis<4,5-dihydroimidazole> 
• 317334-35-3 5-bromo-N₁,N₃-dimethoxy-N₁,N₃-dimethylbenzene-1,3-dicarboxamide 
• 820231-67-2 C₁₆H₂₃BrN₂O₂ 
• 169624-18-4 C₅₂H₆₁BrN₄O₂ 
• 21991-00-4 1,3-dimethyl 5-phenylbenzene-1,3-dicarboxylate 
• 51760-21-5 dimethyl 5-bromoisophthalate 

Relevant academic research and scientific papers

Reversibly Photoswitchable Fluorescent Diarylethenes Resistant against Photobleaching in Aqueous Solutions

Low photostability in aqueous solutions is the main drawback of synthetic photochromic dyes, which limits their switching performance and utility in biology, medicine, and life sciences. Even the most promising photochromes - reversibly photoswitchable di

Effect of alkyl chain length on the extraction properties of U and Th using novel CnmimNTf2/isophthalamide systems

An attempt was made to investigate the structural modification of CnmimNTf2 ionic liquid in combination with a novel ligand, 5-bromo-N1,N3-bis(1-methyl-1H-pyrazol-3-yl)isophthalamide on the extraction properties of tetra and hexavale

Carboxylated Photoswitchable Diarylethenes for Biolabeling and Super-Resolution RESOLFT Microscopy

Reversibly photoswitchable 1,2-bis(2-ethyl-6-phenyl-1-benzothiophene-1,1-dioxide-3-yl)perfluorocyclopentenes (EBT) having fluorescent “closed” forms were decorated with four or eight carboxylic groups and attached to antibodies. Low aggregation, efficient

Sequence-selective assembly of tweezer molecules on linear templates enables frameshift-reading of sequence information

Information storage and processing is carried out at the level of individual macromolecules in biological systems, but there is no reason, in principle, why synthetic copolymers should not be used for the same purpose. Previous work has suggested that mon

Tuning the extraction mechanism of uranyl ion in bicyclooctanium, propylpyridinium, piperidinium and imidazolium based ionic liquids: First ever evidence of 'cation exchange', 'anion exchange' and 'solvation' mechanism

A novel diamide ligand, 5-bromo-N1, N3-diisopropylisophthalamide has been synthesized and characterized by FTIR, 1H NMR, and 13C NMR. The extraction mechanism of uranyl ion with the diamide ligand has been studied in unexplored ionic

Alcohol-Soluble Electron-Transport Materials for Fully Solution-Processed Green PhOLEDs

Two alcohol-soluble electron-transport materials (ETMs), diphenyl(4-(1-phenyl-1H-benzo[d]imidazol-2-yl)phenyl)phosphine oxide (pPBIPO) and (3,5-bis(1-phenyl-1H-benzo[d]imidazol-2-yl)phenyl)diphenylphosphine oxide (mBPBIPO), have been synthesized. The phys

Platform Synthetic Lectins for Divalent Carbohydrate Recognition in Water

Biomimetic carbohydrate receptors (“synthetic lectins”) have potential as agents for biological research and medicine. However, although effective strategies are available for “all-equatorial” carbohydrates (glucose, etc.), the recognition of other types of saccharide under natural (aqueous) conditions is less well developed. Herein we report a new approach based on a pyrene platform with polar arches extending from aryl substituents. The receptors are compatible with axially substituted carbohydrates, and also feature two identical binding sites, thus mimicking the multivalency observed for natural lectins. A variant with negative charges forms 1:2 host/guest complexes with aminosugars, with K1>3000 m?1for axially substituted mannosamine, whereas a positively charged version binds the important α-sialyl unit with K1≈1300 m?1.

Organic light emitting host materials

Disclosed herein are compounds represented by formula: where HT, ET, and R1-R6 are described herein. Compositions of said compounds along with organic light-emitting diode (OLED) devices related thereto are also disclosed.

Tackling poison and leach: Catalysis by dangling thiol-palladium functions within a porous metal-organic solid

Self-standing thiol (-SH) groups within a Zr(iv)-based metal-organic framework (MOF) anchor Pd(ii) atoms for catalytic applications: the spatial constraint prevents the thiol groups from sealing off/poisoning the Pd(ii) center, while the strong Pd-S bond precludes Pd leaching, enabling multiple cycles of heterogeneous catalysis to be executed. This journal is

Synthetic bacteriochlorins bearing polar motifs (carboxylate, phosphonate, ammonium and a short PEG). Water-solubilization, bioconjugation, and photophysical properties

Bacteriochlorins are potentially excellent chromophores for near-infrared (NIR) photochemical and spectroscopic studies yet the intrinsically hydrophobic macrocycle core has stymied work in aqueous media. Herein, a set of bacteriochlorins bearing distinct