Manufacturer Supply with High Purity and Stable Quality
Chemical Name: 4-Fluorobenzeneboronic Acid
Synonyms: 4-Fluorophenylboronic Acid
CAS: 1765-93-1
Appearance: White or Off-White Crystallized Powder
Purity: ≥99.0% (HPLC)
High Quality, Commercial Production
| Chemical Name |
4-Fluorobenzeneboronic Acid |
| Synonyms |
4-Fluorophenylboronic Acid |
| CAS Number |
1765-93-1 |
| CAT Number |
RF-PI231 |
| Stock Status |
In Stock, Production Scale Up to Tons |
| Molecular Formula |
C6H6BFO2 |
| Molecular Weight |
139.92 |
| Melting Point |
262.0~265.0℃ (lit.) |
| Brand |
Ruifu Chemical |
| Item |
Specifications |
| Appearance |
White or Off-White Crystallized Powder |
| Purity / Analysis Method |
≥99.0% (HPLC) |
| Loss on Drying |
≤0.50% |
| Residue on ignition |
≤0.50% |
| Individual Impurity |
≤0.50% |
| Total Impurities |
≤1.0% |
| Test Standard |
Enterprise Standard |
| Usage |
Pharmaceutical Intermediates; Organic Synthesis |
Package: Bottle, Aluminum foil bag, Cardboard drum, 25kg/Drum, or according to customer's requirement.
Storage Condition: Store in sealed containers at cool and dry place; Protect from light, moisture and pest infestation.
Shanghai Ruifu Chemical Co., Ltd. is the leading manufacturer and supplier of 4-Fluorobenzeneboronic Acid (CAS: 1765-93-1) with high quality, widely used in organic synthesis, synthesis of pharmaceutical intermediates and Active Pharmaceutical Ingredient (API) synthesis.
4-Fluorobenzeneboronic Acid (CAS: 1765-93-1) can be used as intermediates of Liquid Crystals and in suzuki reaction.
4-Fluorobenzeneboronic acid was used in the development of effective inhibitors for analog sensitive kinases to study the cellular function of kinases in real time.
4-Fluorophenylboronic acid can be used as a reactant in coupling reactions with arenediazonium tetrafluoroborates, iodonium salts, and iodanes. It is also used to make novel biologically active terphenyls. It can also be used as a reactant in:
Suzuki coupling using microwave and triton B catalyst.
Pd-catalyzed direct arylation of pyrazoles with phenylboronic acids.
Mizoroki-Heck and Suzuki-Miyaura coupling reactions catalyzed by palladium nanoparticles.
Cu-catalyzed Petasis reactions.
Tandem-type Pd(II)-catalyzed oxidative Heck reaction and intramolecular C-H amidation sequence.
Ruthenium catalyzed direct arylation.
Rh-catalyzed asymmetric conjugate additions.
Ligand-free copper-catalyzed coupling of nitro arenes with arylboronic acids.
Regioselective arylation and alkynylation by Suzuki-Miyaura and Sonogashira cross-coupling reactions.
Suzuki cross-coupling of tetrabromothiophene.
Palladium-catalyzed addition to nitriles.