130657-51-1

Basic information

• Product Name: OCTAHYDROCYCLOPENTAL [C] PYRROL-5-AMINE
• Synonyms: OCTAHYDROCYCLOPENTAL [C] PYRROL-5-AMINE;octahydrocyclopenta[c]pyrrol-5-amine;CYCLOPENTA[C]PYRROL-5-AMINE, OCTAHYDRO-, (3AA,5BETA,6AA)-
• CAS NO: 130657-51-1
• Molecular Formula: C7H14N2
• Molecular Weight: 126.202
• Mol File: 130657-51-1.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 205.4°C at 760 mmHg
• Flash Point: 87.7°C
• Appearance: /
• Density: 0.997g/cm³
• Vapor Pressure: 0.25mmHg at 25°C
• Refractive Index: 1.5
• CAS DataBase Reference: OCTAHYDROCYCLOPENTAL [C] PYRROL-5-AMINE(CAS DataBase Reference)
• NIST Chemistry Reference: OCTAHYDROCYCLOPENTAL [C] PYRROL-5-AMINE(130657-51-1)
• EPA Substance Registry System: OCTAHYDROCYCLOPENTAL [C] PYRROL-5-AMINE(130657-51-1)

Safety Data

• Hazardous Substances Data: 130657-51-1(Hazardous Substances Data)

Usage

InChI:InChI=1/C7H14N2/c8-7-1-5-3-9-4-6(5)2-7/h5-7,9H,1-4,8H2

Upstream product

• 130658-21-8 (3aS,4S,6aR)-4-Hydroxy-hexahydro-cyclopenta[c]pyrrole-2-carboxylic acid benzyl ester 
• 130658-18-3 (3aR,5s,6aS)-benzyl 5-((methylsulfonyl)oxy)hexahydrocyclopenta[c]pyrrole-2(1H)-carboxylate 
• 140211-02-5 rac-(3aS,6aR)-benzyl 4-oxohexahydrocyclopenta[c]pyrrole-2(1H)-carboxylate 
• 140211-03-6 (3aS,4R,6aR)-4-Chloro-hexahydro-cyclopenta[c]pyrrole-2-carboxylic acid benzyl ester 
• 130658-19-4 (3aS,6aR)-3,3a,4,6a-Tetrahydro-1H-cyclopenta[c]pyrrole-2-carboxylic acid benzyl ester 
• 130657-82-8 (3aS,5R,6aR)-5-Azido-hexahydro-cyclopenta[c]pyrrole-2-carboxylic acid benzyl ester 

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