130658-09-2

Basic information

• Product Name: Cyclopenta[c]pyrrol-4(1H)-one
• Synonyms: Cyclopenta[c]pyrrol-4(1H)-one;1H,4H-cyclopenta[c]pyrrol-4-one
• CAS NO: 130658-09-2
• Molecular Formula: C₂₆H₂₅NO
• Molecular Weight: 119.1207
• Mol File: 130658-09-2.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 386.052°C at 760 mmHg
• Flash Point: 159.375°C
• Appearance: /
• Density: 1.325g/cm³
• Vapor Pressure: 0mmHg at 25°C
• Refractive Index: 1.671
• CAS DataBase Reference: Cyclopenta[c]pyrrol-4(1H)-one(CAS DataBase Reference)
• NIST Chemistry Reference: Cyclopenta[c]pyrrol-4(1H)-one(130658-09-2)
• EPA Substance Registry System: Cyclopenta[c]pyrrol-4(1H)-one(130658-09-2)

Safety Data

• Hazardous Substances Data: 130658-09-2(Hazardous Substances Data)

Usage

InChI:InChI=1/C7H5NO/c9-7-2-1-5-3-8-4-6(5)7/h1-2,4H,3H2

Upstream product

• 930-30-3 cyclopent-2-enone 
• 115011-73-9 3-(triphenylmethyl)-5-oxazolidinone 

Downstream Products

• 130657-78-2 (3aR,4S,6aS)-2-Trityl-octahydro-cyclopenta[c]pyrrol-4-ylamine 
• 130657-78-2 (3aR,6aS)-2-Trityl-octahydro-cyclopenta[c]pyrrol-4-ylamine 
• 130658-23-0 2-((3aR,4S,6aS)-2-Trityl-octahydro-cyclopenta[c]pyrrol-4-yl)-isoindole-1,3-dione 
• 130657-83-9 N-((3aR,4S,6aS)-2-Trityl-octahydro-cyclopenta[c]pyrrol-4-yl)-acetamide 
• 130657-77-1 (3aR,6aS)-2-Trityl-hexahydro-cyclopenta[c]pyrrol-4-one oxime 
• 130657-76-0 (3aR,4R,6aS)-2-Trityl-octahydro-cyclopenta[c]pyrrol-4-ol 

Relevant articles and documents

Synthesis and antibacterial activity of new 7-(aminoazabicycloalkanyl)quinolonecarboxylic acids

A series of novel 7--6-fluoro-1-substituted quinolinecarboxylic acids (18-53) have been prepared and their antibacterial activities evaluated.These compounds are characterized structurally by a new amino-substituted azabicyclooctane, -nonane and -decane ring systems at the 7-position of quinolonecarboxylic acids.To compare the biological activities of enantiomers, (+)-7-octan-3-yl>-1-cyclopropyl-6,8-difluoro-1,4-dihydro-4-oxo-3-quinolonecarboxylicacid hydrochloride (43, 44) were synthesized and evaluated for antibacterial activity.Compound 43 was more potent than 44 against both Gram-positive and Gram-negative organisms.The structure-activity relationships of these quinolonecarboxylic acids are also discussed. antibacterial activity / amino-substituted azabicycloalkane ring / substituted quinolonecarboxylic acids / structure-activity relationships