1069137-31-0

Usage

Uses

Used in Organic Synthesis:
3-Nitro-2-(pyridin-2-yl)pyridine is used as a key intermediate in organic synthesis for the production of various chemical compounds. Its unique structure allows for the creation of a wide array of molecules with potential applications in different fields.
Used in Medicinal Chemistry Research:
In the realm of medicinal chemistry, 3-Nitro-2-(pyridin-2-yl)pyridine is utilized as a building block in the synthesis of pharmaceuticals. Its presence in the molecular structure can contribute to the development of new drugs with specific therapeutic properties.
Used in Drug Discovery and Development:
3-Nitro-2-(pyridin-2-yl)pyridine is employed as a target in drug discovery and development due to its demonstrated biological activities. Its anti-microbial and anti-cancer properties make it a promising candidate for the creation of new therapeutic agents.
Used in Agrochemicals Synthesis:
3-Nitro-2-(pyridin-2-yl)pyridine is also used in the synthesis of agrochemicals, where it can contribute to the development of pesticides and other agricultural chemicals that are essential for crop protection and yield enhancement.

Upstream product

• 5470-18-8 2-Chloro-3-nitropyridine 
• 197958-29-5 pyridin-2-ylboronic acid 
• 17997-47-6 2-tri-n-butylstannylpyridine 

Downstream Products

• 75449-34-2 5H-pyrrolo<3,2-b:4,5-b'>dipyridine 

Relevant academic research and scientific papers

Diazcarbazole derivative, preparation method thereof, and application of diazcarbazole derivative as electroluminescent material

The invention belongs to the technical field of organic photoelectric material application, and particularly relates to a diazcarbazole derivative with different relative positions of N atoms and an application of the diazcarbazole derivative as an electroluminescent material. Carbazole-like group diazcarbazole with an electron-deficient property is introduced, and a triplet state of the materialcan be realized and the molecular orbital energy level can be adjustable through bonding with different groups, so that efficient recombination of carriers in an organic electroluminescent device is achieved fundamentally, an efficient and energy-saving organic light emitting diode (OLED) device is obtained, and the diazcarbazole derivative can be widely applied to the field of organic electroluminescence. The structural general formula of the material is as shown in the formula I, wherein a same diazcarbazole (diazcarbazole with N positions of 1,8, 1,7, 1,6, 2,7, 2,6, 2,5, 3,6, 3,5, and 4,5)is taken as a core, the L group is a bridging group for bonding the diazlocarbazole, the L group is selected from aromatic groups or aromatic heterocyclic groups containing heteroatoms, m and n are the numbers of the diazicarbazole, and the sum of m and n is greater than or equal to 1.

An efficient route to polynitrogen-fused tricycles via a nitrene-mediated N-N bond formation under microwave irradiation

The synthesis of unprecedented fused azaheterocyclic ring systems is described. Tricycles with either a central pyrazole or a triazole ring were obtained via a nitrene-mediated reaction of nitro bis(hetaryl) derivatives in the presence of triethylphosphite. The cyclization proceeded with complete chemoselectivity for the desired N-N bond formation and was completed within minutes under microwave activation. The key nitro bicycles were synthesized using either Stille couplings or aromatic nucleophilic substitution.