Skip to Content
Merck
All Photos(1)

Key Documents

View All Documentation

Safety Information

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

Sign Into View Organizational & Contract Pricing
All Photos(1)

About This Item

Empirical Formula (Hill Notation):
C4H5BO2S
CAS Number:
6165-69-1
Molecular Weight:
127.96
Beilstein:
113573
MDL number:
MFCD00151851
UNSPSC Code:
12352103
PubChem Substance ID:
24867306
NACRES:
NA.22

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

Other Notes

Contains varying amounts of anhydride

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H302,H315,H319,H335

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

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

PRTR

Class I Designated Chemical Substances

JAN Code

436844-VAR:
436844-1G:
436844-BULK:
436844-5G:

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
SHBK9080
SHBD2264V
40996JMV
40996JM
95998MJ

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Search for a COA

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

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

Suzuki–Miyaura Coupling Reagents

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

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service