182868-20-8

Basic information

• Product Name: C₂₈H₃₀ClN₃O₆
• Synonyms: C₂₈H₃₀ClN₃O₆
• CAS NO: 182868-20-8
• Molecular Weight: 540.016
• Mol File: 182868-20-8.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: C₂₈H₃₀ClN₃O₆(CAS DataBase Reference)
• NIST Chemistry Reference: C₂₈H₃₀ClN₃O₆(182868-20-8)
• EPA Substance Registry System: C₂₈H₃₀ClN₃O₆(182868-20-8)

Safety Data

• Hazardous Substances Data: 182868-20-8(Hazardous Substances Data)

Upstream product

• 182868-16-2 C₂₄H₂₅ClN₂O₆ 
• 182868-09-3 C₂₁H₂₈ClN₃O₄ 
• 182868-14-0 C₂₀H₁₈Cl₂N₂O₄ 
• 182868-12-8 C₂₀H₁₉ClN₂O₅ 
• 182867-99-8 2,6-Dichloro-5-fluoro-N-(2-hydroxy-1,1-dimethyl-ethyl)-nicotinamide 
• 182867-77-2 2,6-Dichloro-3-(4,4-dimethyl-4,5-dihydro-oxazol-2-yl)-5-fluoro-pyridine 
• 501-53-1 benzyl chloroformate 
• 82671-06-5 2,6-dichloro-5-fluoro-3-pyridinecarboxylic acid 
• 96568-02-4 2,6-dichloro-5-fluoro-3-nicotinoyl chloride 
• 765-30-0 Cyclopropylamine 
• 182868-18-4 C₂₇H₂₉ClN₂O₇ 

Downstream Products

• 182868-24-2 C₂₈H₂₉N₃O₆ 

Relevant articles and documents

The synthesis and in vitro antibacterial activity of conformationally restricted quinolone antibacterial agents

Two series of conformationally restricted quinolone antibacterials were synthesized. One series was restricted by formation of a tetrahydrofuran ring between the C-6 position and the C-7 position of the quinolone ring skeleton. The second series achieved conformational rigidity by formation of a tetrahydrofuran ring between the C-7 and the C-8 positions. These compounds were evaluated for their in vitro antibacterial activity. Compounds 19 and 20 were the most active compounds in either series and were about equipotent.