2,3,4,5-Tetrafluorophenylboronic acid
2,3,4,5-Tetrafluorophenylboronic acid (CAS: 179923-32-1) is a specialized organoboronic acid derivative. It is recognised for its utility as a reactant in base-catalyzed hydrodeboration and deuterodeboration reactions, as well as a catalyst in amidation processes. This compound is a key building block in organic synthesis, particularly for introducing tetrafluorophenyl moieties into complex molecules. Available from Tech Serve Solutions, it meets rigorous quality standards for research and chemical manufacturing.
- IUPAC
- 2,3,4,5-Tetrafluorobenzeneboronic acid
- Synonyms
- 2,3,4,5-Tetrafluorophenylboronic acid5-Tetrafluorophenylboronic acidC6H3BF4O2

Reactant in Hydrodeboration
Serves as a reactant in base-catalyzed hydrodeboration and deuterodeboration reactions, enabling specific hydrogen or deuterium incorporation.
Catalyst in Amidation
Functions as a catalyst to facilitate the formation of amide bonds in various chemical syntheses.
Synthetic Intermediate
Utilised as an intermediate in the synthesis of complex organic molecules, particularly those requiring a tetrafluorophenyl group.
| Molecular weight | 193.89 |
|---|---|
| Empirical formula | C6H3BF4O2 |
| Assay | ≥95% |
| Application | Reactant for:• Base-catalyzed hydrodeboration and deuterodeboration1Catalyst for:• Amidation reactions2 |
| Melting point | 264-269 °C |
| Protective equipment | Eyeshields, Gloves, type N95 (US), type P1 (EN143) respirator filter |
|---|---|
| Water hazard class (WGK, DE) | 3 |
Hazard information is provided for guidance. Always consult the product Safety Data Sheet (SDS), available on request, before handling.
Documentation
Every batch ships with a Certificate of Analysis covering assay, identity and purity; the grade is confirmed against your enquiry. Safety Data Sheets and technical data sheets are available on request.
Supply & logistics
Samples for technical evaluation; bulk MOQ by grade and packaging. In-stock material ships in 7–10 working days, worldwide, with full export documentation.
What are the primary uses of 2,3,4,5-Tetrafluorophenylboronic acid?
+
This compound is primarily used as a reactant in hydrodeboration and deuterodeboration reactions and as a catalyst in amidation processes. It is also a valuable intermediate in organic synthesis.
What is the CAS number and formula for 2,3,4,5-Tetrafluorophenylboronic acid?
+
The CAS number is 179923-32-1 and the empirical formula is C6H3BF4O2.
What is the typical purity of 2,3,4,5-Tetrafluorophenylboronic acid supplied by TSS?
+
2,3,4,5-Tetrafluorophenylboronic acid is typically supplied at an assay of ≥95%.
What are the safety considerations when handling 2,3,4,5-Tetrafluorophenylboronic acid?
+
Appropriate personal protective equipment, including eyeshields and gloves, should be worn. A type N95 (US) or type P1 (EN143) respirator filter is recommended. Consult the Safety Data Sheet for full hazard information. Its WGK Germany rating is 3.
How is 2,3,4,5-Tetrafluorophenylboronic acid supplied and exported?
+
Tech Serve Solutions is a global supplier and exporter of 2,3,4,5-Tetrafluorophenylboronic acid, ensuring secure and compliant packaging for international shipment.
How can I request a quote for 2,3,4,5-Tetrafluorophenylboronic acid?
+
To request a quote, please contact our sales team through the website or by phone, providing your specific requirements.
▶ Related products

1-(2-Fluorobenzyl)piperazine
C11H15FN2
Chemical Synthesis
1-(2-Fluorophenyl)biguanide hydrochloride
Chemical Synthesis

1-(2-Fluorophenyl)cyclopropanecarboxylic acid
C10H9FO2
Chemical Synthesis
1-(2-Fluorophenyl)piperazine
C10H13FN2
Chemical Synthesis
1-(2-Fluorophenyl)piperazine monohydrochloride
C10H13FN2 · HCl
Chemical Synthesis
1-(2-Furoyl)-1H-benzotriazole
C11H7N3O2
Chemical Synthesis
1-(2-Furoyl)piperazine
C9H12N2O2
Chemical Synthesis
1-(2-Hydroxy-5-methylphenyl)-3-phenyl-1,3-propanedione
Chemical Synthesis
▶ Explore more

3-Methyl-1,5-di-p-tolyl-1,4-pentazadiene
Chemical Synthesis

3-Methyl-1,5-pentanediol
Chemical Synthesis

3-Methyl-1-(2-methylphenyl)-1H-pyrazol-5-amine
C11H13N3
Chemical Synthesis
3-Methyl-1-(3′-sulfoamidophenyl)-5-pyrazolone
C10H11N3O3S
Chemical Synthesis