80100-16-9

Usage

Uses

Used in Organic Synthesis:
(6-BROMO-PYRIDIN-2-YL)-PHENYL-METHANONE is used as a building block in organic synthesis for its ability to be further functionalized. Its chemical properties and reactivity make it a valuable component in creating a variety of useful derivatives for different applications.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, (6-BROMO-PYRIDIN-2-YL)-PHENYL-METHANONE may be utilized as a key intermediate in the development of new drugs. Its unique structure could be harnessed to design molecules with specific therapeutic properties, potentially leading to the creation of novel medications.
Used in Agrochemicals:
(6-BROMO-PYRIDIN-2-YL)-PHENYL-METHANONE may also find use in the agrochemical sector, where it could serve as a precursor for the synthesis of new pesticides or other agricultural chemicals. Its potential to be modified and functionalized allows for the development of targeted and effective products.
Used in Materials Science:
In the field of materials science, (6-BROMO-PYRIDIN-2-YL)-PHENYL-METHANONE could be explored for its potential to contribute to the development of new materials with specific properties. Its chemical structure may enable the creation of materials with unique characteristics, such as improved stability or reactivity, for various applications.

Upstream product

• 624-28-2 2,5-dibromopyridine 
• 611-74-5 N,N-dimethylbenzamide 
• 740841-42-3 6-bromonicotinoyl chloride 
• 71-43-2 benzene 
• 6311-35-9 6-bromonicotinic acid 
• 93-99-2 benzoic acid phenyl ester 
• 223463-14-7 6-bromopyridin-3-ylboronic acid 
• 591-51-5 phenyllithium 
• 149806-06-4 6-bromonicotinaldehyde 

Downstream Products

• 30091-51-1 5-benzoyl-2-phenylpyridine 
• 1108507-31-8 C₂₂H₂₁NO 
• 1428526-42-4 (6-bromopyridin-3-yl)(phenyl)methanone oxime 
• 1355238-23-1 (6-bromopyridin-3-yl)(phenyl)methylamine 
• 1428526-43-5 tert-butyl N-[(6-bromopyridin-3-yl)(phenyl)methyl]carbamate 
• 1428526-44-6 diethyl (5-{[(tert-butoxycarbonyl)amino](phenyl)methyl}pyridin-2-yl)phosphonate 
• 1428526-45-7 diethyl {5-[amino(phenyl)methyl]pyridin-2-yl}phosphonate 
• 1428526-46-8 diethyl 5-((4-hydroxy-2-(pyridin-2-yl)pyrimidine-5-carboxamido)(phenyl)methyl)pyridin-2-ylphosphonate 
• 1428526-47-9 ethyl hydrogen (5-((4-hydroxy-2-(pyridin-2-yl)pyrimidine-5-carboxamido)(phenyl)methyl)pyridin-2-yl)phosphonate 
• 1428618-76-1 diethyl {5-[amino(phenyl)methyl]pyridin-2-yl}phosphonate 
• 52100-58-0 2,2'-bipyridine-5,5'-diylbis(phenylmethanone) 

Relevant academic research and scientific papers

Pyridine-based thermally activated delayed fluorescent material and application thereof

The invention relates to a pyridine-based thermally activated delayed fluorescent material. The material comprises a compound shown as a formula (I) shown in the specification; and in the formula (I), D is an electron-donating group, and A is an electron-withdrawing group. The pyridine-based thermally activated delayed fluorescence material can be used for preparing organic electroluminescent devices, especially non-doped organic electroluminescent devices, and solves the problems of complex design and existed exciton quenching of the current non-doped thermally activated delayed fluorescent material.

Efficient construction of C–C bonds from aryl halides/aryl esters with arylboronic acids catalysed by palladium(II) thiourea complexes

A new set of palladium(II) complexes comprising phenyl(thiazolyl)thiourea ligands have been successfully synthesized and characterized with the aid of analytical as well as spectral (IR, UV–visible and NMR) methods. A distorted square-planar geometry with N^S coordination mode of thiourea ligands in the new palladium complexes was corroborated by single-crystal X-ray diffraction methods. Interestingly, the palladium(II) thiourea complexes showed the highest catalytic activity with 0.1 mol% catalyst loading in Suzuki–Miyaura cross-coupling reactions utilizing a range of aryl bromides/unactivated aryl chlorides with arylboronic acids as coupling partners in aqueous–organic media. Syntheses of diaryl ketones using aryl esters and arylboronic acids as coupling partners were also achieved with low catalyst loading within 20 h. The potential of our catalyst was demonstrated by its wide substrate scope, low catalyst loadings and high isolated yield. Moreover, the influences of key parameters like solvent, base, temperature and catalyst loading were also investigated.

SUBSTITUTED PYRIMIDINES

The present invention relates to substituted pyrimidines useful as HIF prolyl hydroxylase inhibitors to treat anemia and like conditions.

SUBSTITUTED PYRIMIDINES

Disclosed are substituted pyrimidines useful as HIF prolyl hydroxylase inhibitors to treat anemia and like conditions.

Novel red electroluminescent compounds and organic electronluminescent device using same

The present invention relates to novel red phosphorescent compounds exhibiting high luminous efficiency, and organic electroluminescent devices comprising the same.

Novel red electroluminescent compounds and organic electroluminescent device using the same

The present invention relates to novel red phosphorescent compounds exhibiting high luminous efficiency, and organic electroluminescent devices comprising the same.