Factory Outlets 2-Deoxyguanosine monohydrate - 4-Fluorobenzeneboronic Acid CAS 1765-93-1 Purity ≥99.0% (HPLC) High Purity – Ruifu

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

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.