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436844

Sigma-Aldrich

3-Thienylboronic acid

≥95.0%

Synonyme(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

Formule empirique (notation de Hill):
C4H5BO2S
Numéro CAS:
6165-69-1
Poids moléculaire :
127.96
Numéro Beilstein :
113573
Numéro MDL:
MFCD00151851
Code UNSPSC :
12352103
ID de substance PubChem :
24867306
Nomenclature NACRES :
NA.22

Pureté

≥95.0%

Forme

solid

Pf

164-169 °C (lit.)

Chaîne SMILES 

OB(O)c1ccsc1

InChI

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

Clé InChI

QNMBSXGYAQZCTN-UHFFFAOYSA-N

Autres remarques

Contains varying amounts of anhydride

Pictogrammes

Exclamation mark
GHS07

Mention d'avertissement

Warning

Mentions de danger

H302,H315,H319,H335

Classification des risques

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

Organes cibles

Respiratory system

Code de la classe de stockage

11 - Combustible Solids

Classe de danger pour l'eau (WGK)

WGK 3

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable

Équipement de protection individuelle

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
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Suzuki-Miyaura Cross-Coupling Reagents

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

Suzuki-Miyaura Cross-Coupling Reagents

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

Suzuki-Miyaura Cross-Coupling Reagents

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

Suzuki-Miyaura Cross-Coupling Reagents

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

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