41043-09-8

Basic information

• Product Name: 6,7,8,9-TETRAHYDRO-5H-CYCLOHEPTA[B]PYRIDINE-N-OXIDE
• Synonyms: 6,7,8,9-TETRAHYDRO-5H-CYCLOHEPTA[B]PYRIDINE-N-OXIDE;1-oxido-6,7,8,9-tetrahydro-5H-cyclohepta[b]pyridin-1-ium
• CAS NO: 41043-09-8
• Molecular Formula: C₁₀H₁₃NO
• Molecular Weight: 163.21632
• Mol File: 41043-09-8.mol
• Article Data: 10

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 6,7,8,9-TETRAHYDRO-5H-CYCLOHEPTA[B]PYRIDINE-N-OXIDE(CAS DataBase Reference)
• NIST Chemistry Reference: 6,7,8,9-TETRAHYDRO-5H-CYCLOHEPTA[B]PYRIDINE-N-OXIDE(41043-09-8)
• EPA Substance Registry System: 6,7,8,9-TETRAHYDRO-5H-CYCLOHEPTA[B]PYRIDINE-N-OXIDE(41043-09-8)

Safety Data

• Hazardous Substances Data: 41043-09-8(Hazardous Substances Data)

Upstream product

• 7197-96-8 2,3-cycloheptenopyridine 
• 502-42-1 cycloheptanone 
• 497-19-8 sodium carbonate 

Downstream Products

• 7197-96-8 2,3-cycloheptenopyridine 
• 912277-27-1 (S)-6,7,8,9-tetrahydro-5H-cyclohepta[b]pyridin-9-yl diphenylphosphinite 
• 156601-79-5 2-<(4-methoxy-6,7,8,9-tetrahydro-5H-cycloheptapyridin-9-yl)sulfinyl>-1H-benzimidazole 
• 156601-79-5 2-<(4-methoxy-6,7,8,9-tetrahydro-5H-cycloheptapyridin-9-yl)sulfinyl>-1H-benzimidazole 

Relevant articles and documents

COMPOUNDS AND METHODS FOR TREATING CANCER

Substituted hydrazone compounds, methods of making such compounds and metal complexes thereof, pharmaceutical compositions and medicaments comprising such compounds, and methods of using such compounds and metal complexes to treat, prevent or ameliorate cancer are provided.

Oxidation reactions using polymer-supported 2-benzenesulfonyl-3-(4- nitrophenyl)oxaziridine

A thermally stable polymer-supported oxidant has been developed. Polymer-supported 2-benzenesulfonyl-3-(4-nitrophenyl)oxaziridine was applied to microwave-assisted reactions that occurred at high temperatures and was shown to oxidize alkenes, silyl enol ethers, and pyridines to the corresponding epoxides and pyridine N-oxides in excellent to good yields and with much shorter reaction times. It also enabled tetrahydrobenzimidazoles to be oxidatively rearranged to spiro fused 5-imidazolones in a more efficient manner. Recycling of the polymer-supported oxidant is also possible with minimal loss of activity after several reoxidations.

Iridium catalysts with bicyclic pyridine-phosphinite ligands: Asymmetric hydrogenation of olefins and furan derivatives

(Chemical Equation Presented) Superior bicyclics: Iridium catalysts as 1 derived from pyridine-phosphinite ligands considerably extend the scope of asymmetric hydrogenation. In addition to various unfunctionalized and functionalized olefins, furans, and benzofurans, for which no catalysts were known before, are also hydrogenated with high enantioselectivity (see scheme).