146140-99-0

Usage

Uses

Used in Pharmaceutical Industry:
3-AMINO-4-PHENYLPYRIDINE is used as a key intermediate in the synthesis of various pharmaceuticals for its potential biological activities, including its anti-tumor and anti-inflammatory properties. It contributes to the development of new drugs targeting a range of health conditions.
Used in Agrochemical Industry:
In the agrochemical sector, 3-AMINO-4-PHENYLPYRIDINE serves as a vital building block in the creation of agrochemicals, playing a role in the development of pesticides and other agricultural chemicals to enhance crop protection and yield.
Used in Dye Industry:
3-AMINO-4-PHENYLPYRIDINE is utilized as a chemical intermediate in the production of dyes, contributing to the coloration and performance of various dye products used in different industries such as textiles, plastics, and printing inks.
Used in Organic Chemistry Research:
3-AMINO-4-PHENYLPYRIDINE is employed as a valuable intermediate for the preparation of other nitrogen-containing compounds in organic chemistry, facilitating the exploration of new chemical reactions and the synthesis of novel organic molecules.

InChI:InChI=1/C11H10N2/c12-11-8-13-7-6-10(11)9-4-2-1-3-5-9/h1-8H,12H2

Upstream product

• 131653-64-0 2,2-dimethyl-N-(4-phenyl-3-pyridyl)propanamide 
• 220952-00-1 4-phenyl-3-nitropyridine 
• 239137-39-4 3-amino-4-bromopyridine 
• 98-80-6 phenylboronic acid 
• 13091-23-1 4-chloro-3-nitropyridine 
• 20511-15-3 3-amino-4-chloropyridine 
• 591-50-4 iodobenzene 

Downstream Products

• 1421030-00-3 4-phenyl-3-(3,5-bis(2,4,6-trimethylphenyl)phenyldiazenyl)pyridine 
• 165387-78-0 3-amino-2-chloro-4-phenylpyridine 

Relevant academic research and scientific papers

Additive-free radical cascade reaction of oxime esters: Synthesis of pyrroline-functionalized phenanthridines

A variety of dihydropyrrole-functionalized phenanthridines were efficiently synthesized by the metal-free, radical cascade cyclization reaction of 2-isocyanobiphenyls with γ,δ- unsaturated oxime esters. The C-N/C-C/C-C bonds were formed via the oil bath method in a one-pot procedure with broad substrate applicability. The radical process was supported by kinetic isotope effect studies and radical inhibition studies.

GSK-3 INHIBITORS

The disclosure generally relates to compounds of formula (I), including their salts, as well as compositions and methods of using the compounds to treat disorders associated with GSK-3.

Photocontrol over cooperative porphyrin self-assembly with phenylazopyridine ligands

The cooperative self-assembly of chiral zinc porphyrins is regulated by a photoresponsive phenylazopyridine ligand (1; see picture). Porphyrin stacks depolymerize into dimers upon axial ligation and the strength of the coordination is regulated by its pho

Process for preparing a polyaromatic compound

The present invention concerns a process for preparing a polyaromatic compound comprising a concatenation of two aromatic cycles and carrying at least one amino group on one of the aromatic cycles. The process of the invention is characterized in that it consists of reacting an aromatic compound carrying at least one amino group and a leaving group with an arylboronic acid in an aqueous medium and in the presence of a palladium catalyst.

Preparation of 4-substituted 3-amino-2-chloropyridines, synthesis of a nevirapine analogue

A new method for preparing 3-amino-2-chloropyridines with a substituent (methyl, phenyl, carboxamide, methoxycarbonyl, acetyl, benzoyl and cyano) at the 4-position has been developed. An isoquinoline analogue of the reverse transcriptase inhibitor Nevirapine has been synthesized from the 4-amino-3-chloroisoquinoline.

Connection between metalation and cross-coupling strategies. A new convergent route to azacarbazoles

New convergent synthesis of azacarbazoles through metalation, cross-coupling reaction and intramolecular substitution via (2-aminobenzene)boronic acid and ortho-fluoroiodopyridines.