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It is a biological reagent used as a boronate-assisted fluorogenic chemosensor. It is evaluated for pharmacological activity as fatty acid amide hydrolase inhibitors. It is a reactant involved in coupling with potassium cyanate, quinones, or fluorous tagged N-hydroxyphthalimide and direct C-H arylation of electron-deficient heterocycles.
Hikaru Suenaga, Masafumi Mikami.; K.R.A.Samankumara Sandanayak.; Seiji Shinkai. Screening of fluorescent boronic acids for sugar sensing which show a large fluorescence change.Tetrahedron Lett. 1995, 36 (27), 4825-4828 .
Nicolas DiCesare..; Joseph R. Lakowicz. Spectral Properties of Fluorophores Combining the Boronic Acid Group with Electron Donor or Withdrawing Groups. Implication in the Development of Fluorescence Probes for Saccharides.J. Phys. Chem. A. 2001, 105 (28),6834-6840 .
Fluorescent PET receptor useful in saccharide detection: Tetrahedron Lett., 36, 4825 (1995); Pure Appl. Chem., 68, 2179 (1996). For boronic acid chemistry, see Appendix 5.
Gefahrenhinweise (EU): H315-H319-H335
Causes skin irritation. Causes serious eye irritation. May cause respiratory irritation.
Do not breathe dust/fume/gas/mist/vapours/spray. Obtain special instructions before use. Wear protective gloves. IF INHALED: Remove to fresh air and keep at rest in a position comfortable for breathing. Store locked up. Dispose of contents/container in accordance with local/regional/national/international regulations.