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4-Hydroxyphenylboronic acid, 98%|246703|71597-85-8

4-Hydroxyphenylboronic acid, 98%

Cat. No JK246703_5_G
J&K Chemical

Product Information

Product Name
4-Hydroxyphenylboronic acid, 98%
Brand Name
J&K
Product Number
246703
CAS
71597-85-8
Molecular Formula
C6H7BO3
Molecular Weight
137.93
Certificate of Analysis (COA)​
COA not found

General Information

Synonyms
p-Hydroxyphenylboronic acid
PubChem CID
2734360
IUPAC Name
(4-hydroxyphenyl)boronic acid
InChI Key
COIQUVGFTILYGA-UHFFFAOYSA-N
SMILES
B(C1=CC=C(C=C1)O)(O)O

Properties

Melting Point
>230

Safety Information

Signal Word
Warning
Hazard Statement
H315
H319
H335
Precautionary Statement
P280
P321
P261
P271
P319
P405
P501
P302+P352
P332+P317
P362+P364
P264+P265
P305+P351+P338
P337+P317
P304+P340
P403+P233

References Data Source From Pubchem

Steric confinement-induced emission probe for monitoring protein conformations in live cells
Publication Name: Communications Chemistry
Publication Date: 2026-01-29
DOI: 10.1038/s42004-026-01914-x

Design and synthesis of novel quinazoline derivatives as KDM6B selective inhibitors
Publication Name: Molecular Diversity
Publication Date: 2025-12-19
DOI: 10.1007/s11030-025-11422-0

Bimetallic Cobalt–Silver MOF-Catalyzed Electroreductive Suzuki Coupling in Aqueous Medium Using a Flow Reactor
Publication Name: Arabian Journal for Science and Engineering
Publication Date: 2025-10-10
DOI: 10.1007/s13369-025-10662-4

Structure-based design of alicyclic fused pyrazole derivatives for targeting TGF-β receptor I kinase: molecular docking and dynamics insights
Publication Name: Journal of Computer-Aided Molecular Design
Publication Date: 2025-09-03
DOI: 10.1007/s10822-025-00647-8

Hydrogen Sulfide-Activatable Fluorescence Turn-On Triphenylamine Derivative and Its Application in Real Samples
Publication Name: Journal of Fluorescence
Publication Date: 2025-04-03
DOI: 10.1007/s10895-025-04277-z

4-Hydroxyphenylboronic acid, 98%

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