197724-51-9

Basic information

• Product Name: (E)-2-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)-3-(4-(phenyldiazenyl)phenyl)propanoic acid
• Synonyms: (E)-2-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)-3-(4-(phenyldiazenyl)phenyl)propanoic acid
• CAS NO: 197724-51-9
• Molecular Weight: 491.546
• Mol File: 197724-51-9.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: (E)-2-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)-3-(4-(phenyldiazenyl)phenyl)propanoic acid(CAS DataBase Reference)
• NIST Chemistry Reference: (E)-2-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)-3-(4-(phenyldiazenyl)phenyl)propanoic acid(197724-51-9)
• EPA Substance Registry System: (E)-2-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)-3-(4-(phenyldiazenyl)phenyl)propanoic acid(197724-51-9)

Safety Data

• Hazardous Substances Data: 197724-51-9(Hazardous Substances Data)

Upstream product

• 82911-69-1 N-(9H-fluoren-2-ylmethoxycarbonyloxy)succinimide 
• 949-99-5 4-nitro-3-phenyl-L-alanine 
• 943-80-6 4-amino-L-phenylalanine 
• 154596-15-3 L-phenylalanine-4'-azobenzene 
• 95753-56-3 4-amino-N-[(9H-fluoren-9-ylmethoxy)carbonyl]-L-phenylalanine 
• 586-96-9 Nitrosobenzene 

Relevant articles and documents

Photoswitching of the enzymatic activity of semisynthetic ribonuclease S' bearing phenylazophenylalanine at a specific site

Photos witching of the enzymatic activity of ribonuclease S' was successfully carried out by site specific incorporation of phenylazophenylalanine into S-peptide skeleton by semisynthesis.

Optical switching of ion-dipole interactions in a gramicidin channel analogue

Optical control of ion channel gating could permit the functional manipulation of excitable cells. We wished to examine the feasibility of using optical switching of ion-dipole interactions as a means of switching ion flux in channels. We prepared an anal

Photoswitching of the Enzymatic Activity of Semisynthetic Ribonuclease S' Bearing Phenylazophenylalanine at a Specific Site

Photoswitching of the enzymatic activity of ribonuclease S' was successfully carried out by site specific incorporation of phenylazophenylalanine into S-peptide skeleton by semisynthesis.