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Merck

436844

Sigma-Aldrich

3-Thienylboronic acid

≥95.0%

Sinónimos:

(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

Fórmula empírica (notación de Hill):
C4H5BO2S
Número de CAS:
Peso molecular:
127.96
Beilstein/REAXYS Number:
113573
MDL number:
UNSPSC Code:
12352103
PubChem Substance ID:
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

signalword

Warning

Hazard Classifications

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

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves


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Xu Liang et al.
Dalton transactions (Cambridge, England : 2003), 49(10), 3326-3332 (2020-02-27)
The post-functionalization of six novel symmetric and asymmetric meso-expanded Co(iii) corroles through Suzuki-Miyaura coupling reactions has been successfully accomplished and is reported along with their structural characterization. An analysis of the structure-property relationships of the optical and redox properties of
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
Ingrid Benachio et al.
Journal of molecular recognition : JMR, 34(3), e2878-e2878 (2020-10-07)
Antibiotics, although being amazing compounds, need to be monitored in the environment and foodstuff. This is primarily to prevent the development of antibiotic resistance that may make them ineffective. Unsurprisingly, advances in analyticalsciences that can improve their determination are appreciated.
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

Artículos

Suzuki-Miyaura cross-coupling reaction is extensively used in organic chemistry, polymer science, and pharmaceutical industries.

Suzuki-Miyaura cross-coupling reaction is extensively used in organic chemistry, polymer science, and pharmaceutical industries.

Suzuki-Miyaura cross-coupling reaction is extensively used in organic chemistry, polymer science, and pharmaceutical industries.

Suzuki-Miyaura cross-coupling reaction is extensively used in organic chemistry, polymer science, and pharmaceutical industries.

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