OEM/ODM China (S)-tert-Butyl(5-benzyl-5-azaspiro[2.4]heptan-7-yl)carbamate - 4-Fluorobenzeneboronic Acid CAS 1765-93-1 Purity ≥99.0% (HPLC) High Purity – Ruifu

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OEM/ODM China (S)-tert-Butyl(5-benzyl-5-azaspiro[2.4]heptan-7-yl)carbamate - 4-Fluorobenzeneboronic Acid CAS 1765-93-1 Purity ≥99.0% (HPLC) High Purity – Ruifu Detail:

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.

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