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436844

Sigma-Aldrich

3-Thienylboronic acid

≥95.0%

Synonym(s):

(Thiophene-3-yl)boronic acid, 3-Thiopheneboric acid, 3-Thiopheneboronic acid, 3-Thiophenylboronic acid, Thiophene-3-boronic acid

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About This Item

Empirical Formula (Hill Notation):
C4H5BO2S
CAS Number:
Molecular Weight:
127.96
Beilstein:
113573
MDL number:
UNSPSC Code:
12352103
PubChem Substance ID:
NACRES:
NA.22

Quality Level

Assay

≥95.0%

form

solid

mp

164-169 °C (lit.)

SMILES string

OB(O)c1ccsc1

InChI

1S/C4H5BO2S/c6-5(7)4-1-2-8-3-4/h1-3,6-7H

InChI key

QNMBSXGYAQZCTN-UHFFFAOYSA-N

Related Categories

Other Notes

Contains varying amounts of anhydride

Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

Hazard Classifications

Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

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Muamer Dervisevic et al.
Materials science & engineering. C, Materials for biological applications, 72, 641-649 (2016-12-28)
In this study we report a new, simple and first impedimetric biosensor based on 3-Thienyl boronic acid for dopamine detection. Biosensor electrode preparation is 1min long by simple electro-polymerization of 3-Thienyl boronic acid and copolymer Thiophene P(TBA
Hong-Min Meng et al.
The Analyst, 143(20), 4967-4973 (2018-09-19)
A multifunctional nanosystem, which integrates biosensing, bioimaging, and therapeutic functions into a single nanoprobe, is of great significance for biosensing and biomedicine. Near-infrared (NIR) graphene quantum dots (GQDs) have emerged as an attractive bioimaging and therapy tool for exploring biological
Muamer Dervisevic et al.
Biosensors & bioelectronics, 90, 6-12 (2016-11-21)
The detection of cancer cells through important molecular recognition target such as sialic acid is significant for the clinical diagnosis and treatment. There are many electrochemical cytosensors developed for cancer cells detection but most of them have complicated fabrication processes
Xu Ling et al.
Analytical and bioanalytical chemistry, 410(2), 501-508 (2017-12-29)
A rational-designed conductive sorbent, poly(thiophene-3-boronic acid) electrochemically deposited on a carbon fiber bundle, was applied for boronate affinity extraction. The coated carbon fiber bundle packed into a poly(ether ether ketone) tube was then successfully used for online solid-phase microextraction-high-performance liquid

Articles

This brochure contains a comprehensive selection of boronic acids, boronic acid esters, diboron esters, and transition-metal catalysts useful for the Suzuki–Miyaura coupling reaction

The Suzuki-Miyaura cross-coupling reaction is an important and extensively used reaction in organic chemistry with applications in polymer science and in the fine chemicals and pharmaceutical industries.

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