854616-70-9

Basic information

• Product Name: N-tert-butoxycarbonyl-2-(3-alloxymethyl)phenylpyrrole
• Synonyms: N-tert-butoxycarbonyl-2-(3-alloxymethyl)phenylpyrrole
• CAS NO: 854616-70-9
• Molecular Weight: 313.397
• Mol File: 854616-70-9.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: N-tert-butoxycarbonyl-2-(3-alloxymethyl)phenylpyrrole(CAS DataBase Reference)
• NIST Chemistry Reference: N-tert-butoxycarbonyl-2-(3-alloxymethyl)phenylpyrrole(854616-70-9)
• EPA Substance Registry System: N-tert-butoxycarbonyl-2-(3-alloxymethyl)phenylpyrrole(854616-70-9)

Safety Data

• Hazardous Substances Data: 854616-70-9(Hazardous Substances Data)

Upstream product

• 15852-73-0 (3-Bromophenyl)methanol 
• 854616-68-5 1-allyloxymethyl-3-bromobenzene 
• 854616-69-6 3-(allyloxymethyl)phenylboronic acid 
• 117657-37-1 2-bromo-pyrrole-1-carboxylic acid tert-butyl ester 

Downstream Products

• 854616-71-0 2-(3-allyloxymethyl)phenylpyrrole 

Relevant articles and documents

Highly sodium-selective fluoroionophore based on conformational restriction of oligoethyleneglycol-bridged biaryl boron-dipyrromethene

A non-PET and non-PCT fluoroionophore has been designed and synthesized based on the combination of a biaryl boron-dipyrromethene fluorophore with an oligoethyleneglycol bridge. A specific red-shift response of absorption for NaClO4 in acetonitrile was demonstrated based on conformational restriction triggered by cation recognition at the bridge. The concentration of Na+ can be determined accurately using fluorescence due to a high extinction coefficient (ε = 50000), a high fluorescence quantum yield (Φf = 0.68), and the sharpness of absorption and emission peaks of the boron-dipyrromethene derivative. Copyright