1385032-14-3

Basic information

• Product Name: 1-(4-{[3-(9H-carbazol-4-yloxy)-2-hydroxypropyl]amino}phenyl)ethanone
• Synonyms: 1-(4-{[3-(9H-carbazol-4-yloxy)-2-hydroxypropyl]amino}phenyl)ethanone
• CAS NO: 1385032-14-3
• Molecular Weight: 374.439
• Mol File: 1385032-14-3.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 1-(4-{[3-(9H-carbazol-4-yloxy)-2-hydroxypropyl]amino}phenyl)ethanone(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(4-{[3-(9H-carbazol-4-yloxy)-2-hydroxypropyl]amino}phenyl)ethanone(1385032-14-3)
• EPA Substance Registry System: 1-(4-{[3-(9H-carbazol-4-yloxy)-2-hydroxypropyl]amino}phenyl)ethanone(1385032-14-3)

Safety Data

• Hazardous Substances Data: 1385032-14-3(Hazardous Substances Data)

Upstream product

• 99-92-3 p-aminobenzophenone 
• 51997-51-4 4-(2,3-epoxypropoxy)carbazole 

Downstream Products

• 1385032-15-4 1-{4-[3-(9H-carbazol-4-yloxy)-2-hydroxypropylamino]phenyl}-3-(4-methoxyphenyl)prop-2-enone 
• 1385032-16-5 1-{4-[3-(9H-carbazol-4-yloxy)-2-hydroxypropylamino]phenyl}-3-(2-hydroxyphenyl)prop-2-enone 
• 1385032-17-6 1-{4-[3-(9H-carbazol-4-yloxy)-2-hydroxypropylamino]phenyl}-3-phenylpropen-1-one 
• 1385032-18-7 1-{4-[3-(9H-carbazol-4-yloxy)-2-hydroxypropylamino]phenyl}-3-(2-chlorophenyl)prop-2-enone 
• 1385032-19-8 1-{4-[3-(9H-carbazol-4-yloxy)-2-hydroxypropylamino]phenyl}-3-(4-chlorophenyl)prop-2-enone 
• 1385032-20-1 1-{4-[3-(9H-carbazol-4-yloxy)-2-hydroxypropylamino]phenyl}-3-(3-nitrophenyl)prop-2-enone 
• 1385032-21-2 1-{4-[3-(9H-carbazol-4-yloxy)-2-hydroxypropylamino]phenyl}-3-(4-methoxy-3-nitrophenyl)prop-2-enone 
• 1385032-22-3 1-{4-[3-(9H-carbazol-4-yloxy)-2-hydroxypropylamino]phenyl}-3-(4-methylphenyl)prop-2-enone 
• 1385032-24-5 1-{4-[3-(9H-carbazol-4-yloxy)-2-hydroxypropylamino]phenyl}-3-(4-hydroxyphenyl)prop-2-enone 
• 1385032-25-6 1-{4-[3-(9H-carbazol-4-yloxy)-2-hydroxypropylamino]phenyl}-3-(3,4-dimethoxyphenyl)prop-2-enone 
• 1385032-26-7 1-{4-[3-(9H-carbazol-4-yloxy)-2-hydroxypropylamino]phenyl}-3-(4-nitrophenyl)prop-2-enone 

Relevant articles and documents

Microbial evolution of carbazonyloxy-based chalcones

The Claisen-Schmidt condensation reaction was carried out between a carbazol-based acetyl group and various aldehydes. Reaction was performed in metal alkoxide as a alkali homogenous catalyst. A series of 12 1-{4-[3-(9H-carbazol-4-yloxy)-2-hydroxy-propylamino]-phenyl}-3-(substituted aryl)-propenone were synthesized and characterized using FTIR, 1H NMR, and 13C NMR spectroscopy analysis. Synthesized compounds were tested against bacteria and fungi strains.