CONTACT US

Email: info@alfa-chemistry.com
Tel:1-201-478-8534
1-516-662-5404
Fax: 1-516-927-0118
Address: 2200 Smithtown Avenue, Room 1 Ronkonkoma, NY 11779-7329 USA

For product inquiries, please use our online system or send an email to
inquiry@alfa-chemistry.com

chemistry partner
Home > Product > Boronic Compounds > Boronic Acids > 2,4,6-Trifluorophenylboronic acid

2,4,6-Trifluorophenylboronic acid

Catalog Number
ACM182482253
Product Name
2,4,6-Trifluorophenylboronic acid
Structure
CAS Number
182482-25-3
Synonyms
2,4,6-TRIFLUOROBENZENEBORONIC ACID;2,4,6-TRIFLUOROPHENYLBORONIC ACID;RARECHEM AH PB 0121;2,4,6-Trifluoronenzeneboronic acid;2,4,6-Trifluorophenylboronic;2,4,6-Trifluorophenylboronic Acid (contains varying aMounts of Anhydride);Trifluorobenzeneboronic aci
Molecular Formula
C6H4BF3O2
Molecular Weight
175.9
If you have any other questions or need other size, please get a quote.
  • CAS
  • Size
  • Purity
  • Price
  • Availability
  • Quantity
  • Order
1Organoboron compounds as Lewis acid receptors of fluoride ions in polymeric membranes.

Jańczyk M1, Adamczyk-Woźniak A, Sporzyński A, Wróblewski W.

Anal Chim Acta. 2012 Jul 6;733:71-7. doi: 10.1016/j.aca.2012.04.037. Epub 2012 May 7.

Newly synthesized organoboron compounds - 4-octyloxyphenylboronic acid (OPBA) and pinacol ester of 2,4,6-trifluorophenylboronic acid (PE-PBA) - were applied as Lewis acid receptors of fluoride anions. Despite enhanced selectivity, the polymer membrane electrodes containing the lipophilic receptor OPBA exhibited non-Nernstian slopes of the responses toward fluoride ions in acidic conditions. Such behavior was explained by the lability of the B-O bond in the boronic acids, and the OH(-)/F(-) exchange at higher fluoride content in the sample solution. Read More

Share

Interested in our Services & Products ? Need detailed information?
facebook twitter linkedin google+

Contact us

Email:
Tel:1-201-478-8534
1-516-662-5404
Fax: 1-516-927-0118
Address: 2200 Smithtown Avenue, Room 1 Ronkonkoma, NY 11779-7329 USA