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514055

Sigma-Aldrich

5-Formyl-2-thienylboronic acid

≥95.0%

Sinónimos:

5-Formyl-2-thiopheneboronic acid

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About This Item

Fórmula empírica (notación de Hill):
C5H5BO3S
Número de CAS:
4347-33-5
Peso molecular:
155.97
MDL number:
MFCD02093666
UNSPSC Code:
12352103
PubChem Substance ID:
24873737
NACRES:
NA.22

assay

≥95.0%

mp

132-135 °C (lit.)

SMILES string

[H]C(=O)c1ccc(s1)B(O)O

InChI

1S/C5H5BO3S/c7-3-4-1-2-5(10-4)6(8)9/h1-3,8-9H

InChI key

DEQOVKFWRPOPQP-UHFFFAOYSA-N

Categorías relacionadas

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

Certificados de análisis (COA)

Busque Certificados de análisis (COA) introduciendo el número de lote del producto. Los números de lote se encuentran en la etiqueta del producto después de las palabras «Lot» o «Batch»

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Sigma-Aldrich

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Sigma-Aldrich

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Photochemistry and photobiology, 95(1), 280-292 (2018-07-11)
The synthesis, photophysical and photoacoustic characterization for a series of nine π-extended quadrupolar curcumin dyes is presented. A systematic evaluation of the π-bridging unit including the p-phenyl, naphth-4-yl, thien-2-yl and hybrid 4-naphthathien-2-yl groups is presented. Furthermore, evaluation of the strongly
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ACS omega, 3(10), 12893-12904 (2018-11-10)
A series of push-pull heterocyclic N,N-diphenylhydrazones were prepared to study the effect of structural modifications (different π-spacers and electron-withdrawing groups) on the optical (linear and nonlinear) and electronic properties of the molecules. The photovoltaic response of dye-sensitized solar cells assembled
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Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 202, 196-206 (2018-05-23)
Five isoindigo-based donor-acceptor-donor (D-A-D) type small molecules have been synthesized in order to investigate their intramolecular charge transfer characteristics. UV-vis absorption of these dyes exhibits a wide absorption band ranging from 300 to 650 nm with two distinct bands, giving the
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In an approach to develop efficient organic optoelectronic devices to be used in light-driven systems, a series of three thiophene linked benzimidazole conjugates were synthesized and characterized. The combination of two thiophene rings to a benzimidazole core decorated with different

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