72666-44-5

Usage

General Description

2-(4-chlorophenyl)-6-(4-methoxyphenyl)-4-phenylpyridine, also known as "Larotaxel," is a chemical compound belonging to the pyridine group. It is an anticancer drug and belongs to the class of taxane drugs, which are used in the treatment of various types of cancers, including breast, ovarian, and lung cancers. Larotaxel works by inhibiting the growth of cancer cells and preventing them from dividing and multiplying. It is still under investigation for its potential therapeutic uses and is being studied for its efficacy and safety in different cancer treatments.

Upstream product

• 22966-19-4 trans-4'-methoxychalcone 
• 57269-96-2 2-(2-(4-chlorophenyl)-2-oxoethyl)isoquinolin-2-ium bromide 
• 956-02-5 4'-chlorochalcone 
• 100-06-1 1-(4-methoxyphenyl)ethanone 
• 2475-92-5 4-methoxyacetophenone oxime 
• 184849-67-0 1-(4-chlorophenyl)ethanone O-acetyl oxime 
• 96155-57-6 1-(4-methoxyphenyl)ethanone O-acetyl oxime 
• 100-52-7 benzaldehyde 

Relevant academic research and scientific papers

Copper-Catalyzed coupling of oxime acetates with aldehydes: A new strategy for synthesis of pyridines

Copper-catalyzed coupling of oxime acetates with aldehydes offers a new strategy for the synthesis of highly substituted pyridines. This novel method tolerates a wide range of functionality and allows for rapid elaboration of the oxime acetates into a variety of substituted pyridines.

Pyrylium Compounds. XXI. - Structure and Tautomerism of Pseudobases of Unsymmetrically Substituted 2,4,6-Triarylpyrylium Salts

Hydrolytic ring opening of unsymmetrically substituted 2,4,6-triarylpyrylium salts 11 results in a mixture of two tautomeric pseudobases, the penten-1,5-diones 13 and 14.In crystalline state as a rule one of these tautomers markedly predominates, whereas

Studies on Cycloimmonium Ylides. Synthesis of Some 2,4,6-Triaryl-Substituted Pyridines via Isoquinolinium Ylides

(Aroylmethylene)isoquinolinium ylides on their reaction with different α,β-unsaturated ketones gave a wide variety of 2,4,6-triaryl-substituted pyridines which are expected to possess some potential biological activities.The reaction seemed to proceed via