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Quinoline-3-boronic acid, 97%|264520|191162-39-7

Quinoline-3-boronic acid, 97%

Cat. No JK264520_1_G
J&K Chemical

Product Information

Product Name
Quinoline-3-boronic acid, 97%
Brand Name
J&K
Product Number
264520
CAS
191162-39-7
Molecular Formula
C9H8BNO2
Molecular Weight
172.98
Certificate of Analysis (COA)​
COA not found

General Information

Synonyms
(3-Quinolinyl)boronic acid
PubChem CID
2734663
IUPAC Name
quinolin-3-ylboronic acid
InChI Key
YGDICLRMNDWZAK-UHFFFAOYSA-N
SMILES
B(C1=CC2=CC=CC=C2N=C1)(O)O

Properties

Melting Point
148-155

Safety Information

GHS Symbols
Hazard Symbol
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
Storage Condition
Store at 2-8℃

References Data Source From Pubchem

Methods for the Synthesis of Nitroquinolines (A Review)
Publication Name: Russian Journal of Organic Chemistry
Publication Date: 2025-11
DOI: 10.1134/s1070428025604480

Utilization of Fe3O4@MgO as a heterogeneous solid-base in functional group transformations of arylboronic acids, phenols and benzonitriles
Publication Name: Journal of Chemical Sciences
Publication Date: 2025-01-09
DOI: 10.1007/s12039-024-02333-y

Heck Cross Coupling of On-DNA 4-Vinylbenzamides and Acrylamides with Arylboronic Acid Derivatives
Publication Name: Science of Synthesis
Publication Date: 2024

Copper catalysis in the synthesis of N-naphthyl and N-quinolinyl derivatives of adamantane-containing amines
Publication Name: Russian Chemical Bulletin
Publication Date: 2023-11
DOI: 10.1007/s11172-023-4065-x

Sulfonium-Salt Based Trifluoromethylating Reagent Permits Multiple Reactivity Paradigms
Publication Name: Synfacts
Publication Date: 2021-12-17
DOI: 10.1055/s-0041-1737218

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