113003-48-8

Upstream product

• 113003-47-7 3-Oxo-1-phenyl-3-(3-methylpyridin-4-yl)-propan 
• 583-58-4 3,4-Lutidin 
• 103-63-9 1-phenyl-2-bromoethane 
• 7584-05-6 3-methyl-4-cyanopyridine 

Downstream Products

• 113018-67-0 1,3-dimethyl-4-(3-phenylpropyl)-1,2,5,6-tetrahydropyridine 

Relevant academic research and scientific papers

Synthesis and antifungal activity of novel aza-D-homosteroids, hydroisoquinolines, pyridines and dihydropyridines

A series of novel aza-D-homosteroids and their hydroisoquinoline precursors were synthesized and tested for antifungal activity against a variety of Candida strains and also Aspergillus species. A number of 4-substituted pyridines and tetrahydropyridines

Pyridine derivatives and insecticide and miticide comprising said derivatives

A pyridine compound of the formula STR1 wherein X is a hydrogen atom, a halogen atom, an alkyl group having 1 to 4 carbon atoms, an alkoxyl group having 1 to 4 carbon atoms, a haloalkyl group having 1 to 4 carbon atoms or a haloalkoxyl group having 1 to 4 carbon atoms, n is 1 to 5, and when n is 2 or more, Xs may be identical to or different from each other, A is an alkyl residue or alkene residue in which a portion connecting the aryl group with the 4-position of the pyridyl group has 3 to 8 carbon atoms, or an alkapolyene residue in which said portion has 4 to 8 carbon atoms and 2 to 4 double bonds; the alkyl residue, alkene residue, and alkapolyene residue may have an alkyl side chain having 1 to 4 carbon atoms, an alkylidene side chain having 1 to 4 carbon atoms or 1 to 16 halogen atoms, and when there are 2 or more side chains, the side chains may be identical to or different from each other, and R1 and R2 are each a hydrogen atom or an alkyl group having 1 to 6 carbon atoms or salts thereof. The pyridine compounds and salts thereof exhibit a strong insecticidal and miticidal activity and are low in residuality and accumulativity and are thus useful as insecticides and miticides for the control of pests in agriculture and horticulture.

Intramolecular Alkylations of Aromatic Compounds, XVIII: Synthesis of 3,4-Dihydro-1'-methylspiro

Refluxing the tetrahydroyridines 10 in hydrobromic acid gives the title compounds 12 stereoselectively.Their structures and configurations were confirmed by NMR spectroscopy and X-ray analysis.The tetrahydropyridines 10 were prepared from the pyridinecarbonitriles 5 and Grignard reagents 6 by standard methods.