41318-73-4

Usage

Uses

Used in Pharmaceutical Industry:
Benzene, 1-bromo-3,5-diphenoxyis utilized as an intermediate in the synthesis of pharmaceuticals for its ability to contribute to the development of new drugs with specific therapeutic properties. Its unique structure allows for the creation of molecules with targeted actions against various diseases and conditions.
Used in Agrochemical Industry:
In the agrochemical sector, Benzene, 1-bromo-3,5-diphenoxyserves as a precursor in the production of agrochemicals, potentially enhancing crop protection and management through the development of new pesticides or herbicides.
Used in Dye and Pigment Production:
Benzene, 1-bromo-3,5-diphenoxyis also employed as a precursor in the manufacturing of dyes and pigments, where its chemical structure contributes to the creation of vibrant and stable colorants for various applications, including textiles, plastics, and printing inks.
Safety Measures:
Given the toxic nature of Benzene, 1-bromo-3,5-diphenoxy-, it is crucial to adhere to strict safety protocols during its handling and use. This includes wearing appropriate personal protective equipment, such as gloves and safety goggles, to prevent skin and eye contact. Additionally, proper ventilation should be ensured to minimize inhalation risks, and accidental ingestion or exposure should be avoided at all costs.

Upstream product

• 626-39-1 1,3,5-trisbromobenzene 
• 100-67-4 potassium phenolate 
• 20469-65-2 1-bromo-3,5-dimethoxybenzene 
• 100-39-0 benzyl bromide 
• 461-96-1 3,5-difluorobromobenzene 
• 108-95-2 phenol 

Relevant academic research and scientific papers

One-Step Borylation of 1,3-Diaryloxybenzenes Towards Efficient Materials for Organic Light-Emitting Diodes

The development of a one-step borylation of 1,3-diaryloxybenzenes, yielding novel boron-containing polycyclic aromatic compounds, is reported. The resulting boron-containing compounds possess high singlet-triplet excitation energies as a result of localized frontier molecular orbitals induced by boron and oxygen. Using these compounds as a host material, we successfully prepared phosphorescent organic light-emitting diodes exhibiting high efficiency and adequate lifetimes. Moreover, using the present one-step borylation, we succeeded in the synthesis of an efficient, thermally activated delayed fluorescence emitter and boron-fused benzo[6]helicene.

POLYCYCLIC AROMATIC COMPOUND

PROBLEM TO BE SOLVED: To provide a compound useful as a material for organic devices such as organic electroluminescent elements. SOLUTION: The present disclosure provides a polycyclic aromatic compound of formula (1), where A ring, B ring, C ring, D ring

Organic electroluminescent materials and devices

The invention relates to organic electroluminescent materials and devices. Provided are boron-containing compounds. Also provided are formulations comprising these boron-containing compounds. Further provided are OLEDs and related consumer products that utilize these boron-containing compounds.

ORGANIC ELECTROLUMINESCENT MATERIALS AND DEVICES

Provided are boron-containing compounds. Also provided are formulations comprising these boron-containing compounds. Further provided are OLEDs and related consumer products that utilize these boron-containing compounds.

SECOND GENERATION GRP94-SELECTIVE INHIBITORS

The present technology provides compounds selective for the Grp94 isoform, as well as compositions including such compounds, that are useful for treatment of multiple myeloma, melanoma, lung cancer, hepatocellular carcinoma, breast cancer, prostate cancer

Polycyclic aromatic compound

The present invention addresses the problem of providing a novel polycyclic aromatic compound and an organic electroluminescent element using the same. The above problem is solved by providing a novel polycyclic aromatic compound in which a plurality of aromatic rings are connected by boron atoms, oxygen atoms, or the like, thereby increasing the number of options for organic EL element materials, and also solved by providing a superior organic EL element using said novel polycyclic aromatic compound as an organic EL element material.