116178-39-3

Basic information

• Product Name: 3-Pyridinol,6-ethoxy-(9CI)
• Synonyms: 3-Pyridinol,6-ethoxy-(9CI);2-ethoxy-5-hydroxypyridine
• CAS NO: 116178-39-3
• Molecular Formula: C₇H₉NO₂
• Molecular Weight: 139.15186
• Product Categories: PYRIDINE
• Mol File: 116178-39-3.mol
• Article Data: 4

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 3-Pyridinol,6-ethoxy-(9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: 3-Pyridinol,6-ethoxy-(9CI)(116178-39-3)
• EPA Substance Registry System: 3-Pyridinol,6-ethoxy-(9CI)(116178-39-3)

Safety Data

• Hazardous Substances Data: 116178-39-3(Hazardous Substances Data)

Upstream product

• 116178-33-7 5-ethoxy-1,4-oxazepine 
• 4432-69-3 3-Oxo-2-azabicyclo<2.2.0>hex-5-ene 
• 116178-27-9 1,4-oxazepin-5-one 
• 116178-12-2 2-(tert-butyldimethylsilyl)-2-azabicyclo<2.2.0>hex-5-en-3-one 
• 116178-20-2 3-Oxa-6-aza-tricyclo[3.2.0.0^2,4]heptan-7-one 
• 116178-15-5 6-(tert-Butyl-dimethyl-silanyl)-3-oxa-6-aza-tricyclo[3.2.0.0^2,4]heptan-7-one 
• 142-08-5 2-Pyridone 
• 116178-20-2 6-aza-3-oxatricyclo<3.2.0.0^2,4>heptan-7-one 
• 132433-20-6 1-(methoxymethyl)pyridin-2(1H)-one 
• 132433-25-1 2-methoxymethyl-2-azabicyclo<2.2.0>hex-5-en-3-one 
• 132433-52-4 4-hydroxymethyl-1,4-oxazepin-5-one 
• 132433-40-0 4-methoxymethyl-1,4-oxazepin-5-one 
• 132433-30-8 6-methoxymethyl-6-aza-3-oxatricyclo<3.2.0.0^2,4>heptan-7-one 
• 116178-15-5 6-(tert-butyldimethylsilyl)-6-aza-3-oxatricyclo<3.2.0.0^2,4>heptan-7-one 

Downstream Products

• 5154-01-8 2,5-dihydroxypyridine 

Relevant articles and documents

PYRROLIDINONE DERIVATIVES AS GPR119 MODULATORS FOR THE TREATMENT OF DIABETES, OBESITY, DYSLIPIDEMIA AND RELATED DISORDERS

The present invention relates to pyrrolidinone derivatives. The pyrrolidinone derivatives are GPR119 modulators and useful for the prevention and/or treatment of diabetes, obesity, dyslipidemia and related disorders. The invention furthermore relates to t

Studies on seven-membered heterocycles. XXXI. Synthesis of 1,4-oxazepinones and 1,4-diazepinones from 2-pyridones and their conversion into fully unsaturated 1,4-oxazepines and 1,4-diazepines

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