Bio-Connect
Chemical Structure
Chemical Structure
Chemical Structure

ZnAF-1F Solution [443302-08-7]

Research Use Only
CDX-Z0509
Chemodex
CAS Number443302-08-7
Product group Chemicals
Estimated Purity>90%
Molecular Weight608.59
Price on request
Packing Size
Large volume orders?
Order with a bulk request

Overview

  • Supplier
    Chemodex
  • Product Name
    ZnAF-1F Solution [443302-08-7]
  • Delivery Days Customer
    10
  • CAS Number
    443302-08-7
  • Certification
    Research Use Only
  • Concentration
    5mM
  • Estimated Purity
    >90%
  • Hazard Information
    Non-hazardous
  • Molecular Formula
    C34H26F2N4O5
  • Molecular Weight
    608.59
  • Scientific Description
    Chemical. CAS: 443302-08-7. Formula: C34H26F2N4O5. MW: 608.59. Synthetic. ZnAF-1F and ZnAF-2F do not fluoresce in the presence of other biologically important cations such as Ca2+ and Mg2+, and are insensitive to change of pH. The complexes with Zn2+ of previously developed ZnAFs, ZnAF-1, and ZnAF-2 decrease in fluorescence intensity below pH 7.0 owing to protonation of the phenolic hydroxyl group of fluorescein, whose pKa value is 6.2. On the other hand, the Zn2+ complexes of ZnAF-1F and ZnAF-2F emit stable fluorescence under neutral and slightly acidic conditions because the pKa values are shifted to 4.9 by substitution of electron-withdrawing fluorine at the ortho position of the phenolic hydroxyl group. Spectral data: lambdaex 492nm; lambdaem 517nm in PBS. - ZnAF-1F and ZnAF-2F do not fluoresce in the presence of other biologically important cations such as Ca2+ and Mg2+, and are insensitive to change of pH. The complexes with Zn2+ of previously developed ZnAFs, ZnAF-1, and ZnAF-2 decrease in fluorescence intensity below pH 7.0 owing to protonation of the phenolic hydroxyl group of fluorescein, whose pKa value is 6.2. On the other hand, the Zn2+ complexes of ZnAF-1F and ZnAF-2F emit stable fluorescence under neutral and slightly acidic conditions because the pKa values are shifted to 4.9 by substitution of electron-withdrawing fluorine at the ortho position of the phenolic hydroxyl group. Spectral data: lambdaex 492nm; lambdaem 517nm in PBS.
  • SMILES
    OC1=CC2=C(C=C1F)C1(OC(=O)C3=C1C=CC(NCCN(CC1=CC=CC=N1)CC1=NC=CC=C1)=C3)C1=CC(F)=C(O)C=C1O2
  • Storage Instruction
    2°C to 8°C,-20°C
  • UNSPSC
    12352200