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3-Formyl-2-thienylboronic acid, 98%|217021|17303-83-2

3-Formyl-2-thienylboronic acid, 98%

Cat. No JK217021_1_G
J&K Chemical

Product Information

Product Name
3-Formyl-2-thienylboronic acid, 98%
Brand Name
J&K
Product Number
217021
CAS
17303-83-2
Molecular Formula
C5H5BO3S
Molecular Weight
155.97
SDS Document
View/Download
Certificate of Analysis (COA)​
COA not found

General Information

PubChem CID
2773429
IUPAC Name
(3-formylthiophen-2-yl)boronic acid
InChI Key
HYXMHAHVUFTVFZ-UHFFFAOYSA-N
SMILES
B(C1=C(C=CS1)C=O)(O)O

Properties

Melting Point
330

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

References Data Source From Pubchem

An Efficient Synthesis of 3-Phosphorylated Benzoxaboroles via the Pudovik Reaction
Publication Name: Synthesis
Publication Date: 2017-03-14
DOI: 10.1055/s-0036-1588739

Desymmetrization of meso-Bicyclic Hydrazines: An Efficient Strategy towards the Synthesis of Functionalized Cyclopentenes
Publication Name: Synlett
Publication Date: 2009-10-13
DOI: 10.1055/s-0029-1218287

Structure-based enhancement of boronic acid-based inhibitors of AmpC beta-lactamase
Publication Name: Journal of Medicinal Chemistry
Publication Date: 1998-10-13
DOI: 10.1021/jm980343w

Synthesis of Polyfused Heteroaromatics by Palladium-Catalyzed Cross-Coupling Reaction
Publication Name: Molecules
Publication Date: 1997-02-28
DOI: 10.1007/s007830050042

The versatile chemistry of thiophene. Some contributions by the Gronowitz' group
Publication Name: Chemistry of Heterocyclic Compounds
Publication Date: 1994-11
DOI: 10.1007/bf01172861

3-Formyl-2-thienylboronic acid, 98%

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