4-Fluorophenylboronic acid, 98%

Name: 4-Fluorophenylboronic acid, 98% | 1765-93-1
Brand: J&K Chemical
SKU: JK168063_1_G
Price: 10.0 USD
Availability: OutOfStock

Cat. No JK168063_1_G

Vendor: J&K Chemical

Product Information

Product Name

4-Fluorophenylboronic acid, 98%

Brand Name

J&K

Product Number

168063

CAS

1765-93-1

Molecular Formula

C6H6BFO2

Molecular Weight

139.92

SDS Document

View/Download

Certificate of Analysis (COA)

COA not found

General Information

Synonyms

4-Fluorophenyl)dihydroxyboron 4-Fluorobenzeneboronic acid

PubChem CID

285645

IUPAC Name

(4-fluorophenyl)boronic acid

InChI Key

LBUNNMJLXWQQBY-UHFFFAOYSA-N

SMILES

B(C1=CC=C(C=C1)F)(O)O

Properties

Melting Point

262-265

Safety Information

Signal Word

Warning

Hazard Statement

H302

H315

H319

H335

Precautionary Statement

P270

P330

P501

P280

P321

P261

P271

P319

P405

P301+P317

P302+P352

P332+P317

P362+P364

P264+P265

P305+P351+P338

P337+P317

P304+P340

P403+P233

References

Development of a CYP11B2 imaging tracer for primary aldosteronism: basic evaluation of iodine- and fluorine-incorporated pyridinyldihydroquinolinone derivatives

Publication Name: EJNMMI Radiopharmacy and Chemistry

Publication Date: 2025-07-06

DOI: 10.1186/s41181-025-00361-8

A selenoxide for single-atom protein modification of tyrosine residues enabled by water-resistant chalcogen and hydrogen bonding

Publication Name: Nature Chemistry

Publication Date: 2025-06-04

DOI: 10.1038/s41557-025-01842-8

Catalytic Properties of the Palladium(II) Coordination Polymer in the Reaction of C–C Coupling of Aromatic Halides and Boronic Acids

Publication Name: Theoretical and Experimental Chemistry

Publication Date: 2024-09

DOI: 10.1007/s11237-025-09828-w

Preparation of arylboronic and diarylborinic acids from potassium aryl(fluoro)borates

Publication Name: Monatshefte für Chemie - Chemical Monthly

Publication Date: 2024-05-07

DOI: 10.1007/s00706-024-03213-4

Chelation enables selectivity control in enantioconvergent Suzuki–Miyaura cross-couplings on acyclic allylic systems

Publication Name: Nature Chemistry

Publication Date: 2024-02-08

DOI: 10.1038/s41557-023-01430-8

4-Fluorophenylboronic acid, 98%

Product Information

General Information

Properties

Safety Information

References

Development of a CYP11B2 imaging tracer for primary aldosteronism: basic evaluation of iodine- and fluorine-incorporated pyridinyldihydroquinolinone derivatives

A selenoxide for single-atom protein modification of tyrosine residues enabled by water-resistant chalcogen and hydrogen bonding

Catalytic Properties of the Palladium(II) Coordination Polymer in the Reaction of C–C Coupling of Aromatic Halides and Boronic Acids

Preparation of arylboronic and diarylborinic acids from potassium aryl(fluoro)borates

Chelation enables selectivity control in enantioconvergent Suzuki–Miyaura cross-couplings on acyclic allylic systems