79568-05-1

Upstream product

• 5424-19-1 3-Benzoylpyridine 
• 10400-19-8 3-pyridinecarbonyl chloride 
• 71-43-2 benzene 
• 99-61-6 3-nitro-benzaldehyde 
• 626-55-1 3-Bromopyridine 
• 141307-10-0 (3-nitrophenyl )(pyridin-3-yl)methanol 

Downstream Products

• 79568-06-2 3-(3-aminobenzoyl)pyridine 
• 82465-63-2 5-(3-Nitrobenzoyl)-2-pyridincarboxamid 
• 93943-86-3 (E)-7-(3-Nitro-phenyl)-7-pyridin-3-yl-hept-6-enoic acid 
• 223754-36-7 (3-nitrophenyl)-(3-pyridyl)-ketoxime 
• 221456-47-9 5-[1-(3-Amino-phenyl)-1-pyridin-3-yl-meth-(E)-ylideneaminooxy]-pentanoic acid ethyl ester 
• 223754-37-8 O-(4-ethoxycarbonylbutyl)-(3-nitrophenyl)-(3-pyridyl)ketoxime 
• 1604834-26-5 C₂₂H₁₉N₃O₃ 
• 79567-87-6 [(Z)-3-(3-Fluoro-phenyl)-3-pyridin-3-yl-allyl]-dimethyl-amine 
• 95713-44-3 [(E)-3-(3-Fluoro-phenyl)-3-pyridin-3-yl-allyl]-dimethyl-amine 
• 79568-07-3 (3-fluorophenyl)(pyridin-3-yl)methanone 

Relevant academic research and scientific papers

Preparation and evaluation of arylazide-substituted pyridine adenine dinucleotides for photoaffinity labeling experiments

Two pyridine-modified NAD + analogs, 3-(3-azido benzoyl) pyridine adenine dinucleotide 1 and N-(S-azido-5-carboxyl) phenyl nicotinamide adenine dinucleotide 2 have been prepared and evaluated for photoaffinity labeling experiments. The syntheses were acco

NOVEL PROPENOHYDROXAMIC ACID DERIVATIVES

Provided are a propenohydroxamic acid derivative represented by the following formula (1): [wherein, R1 represents a hydrogen atom, an alkyl group or a halogen atom, R2 represents a cycloalkyl group, a substituted or unsubstituted ar

Approach to dual-acting platelet activating factor (PAF) receptor antagonist/thromboxane synthase inhibitor (TxSI) based on the link of PAF antagonists and TxSIs

A series of compounds (22-36) which possess dual-acting PAF antagonist/TxSI have been generated by the approach of linking the known PAF antagonists and TxIs, such as Ridogrel (1).

A New Simple Synthesis of Fusaric Acid and Other 5-Alkyl-2-pyridinecarboxylic Acids

Carboxamido groups are introduced into the 6-position of 3-acylpyridines with high regioselectivity via Minisci reaction with formamides, Fe(II) sulfate and tert-butyl hydroperoxide.The isolation procedure is considerably improved by the addition of citric acid for complexation of the Fe ions.Fusaric acid and other 5-alkyl-2-pyridine carboxylic acids are obtained by a following Wolff-Kishner reaction in 20-75percent overall yield.