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T32409

Sigma-Aldrich

2-Thiophenecarboxaldehyde

98%

Synonym(s):

Thenaldehyde

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About This Item

Empirical Formula (Hill Notation):
C5H4OS
CAS Number:
98-03-3
Molecular Weight:
112.15
Beilstein/REAXYS Number:
105819
EC Number:
202-629-8
MDL number:
MFCD00005429
UNSPSC Code:
12352100
PubChem Substance ID:
24900117
NACRES:
NA.22

assay

98%

refractive index

n20/D 1.591 (lit.)

bp

198 °C (lit.)
75-77 °C/11 mmHg (lit.)

density

1.2 g/mL at 25 °C (lit.)

storage temp.

2-8°C

SMILES string

[H]C(=O)c1cccs1

InChI

1S/C5H4OS/c6-4-5-2-1-3-7-5/h1-4H

InChI key

CNUDBTRUORMMPA-UHFFFAOYSA-N

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pictograms

Exclamation mark
GHS07

signalword

Warning

hcodes

H302

Hazard Classifications

Acute Tox. 4 Oral

Storage Class

10 - Combustible liquids

wgk_germany

WGK 3

flash_point_f

170.6 °F - closed cup

flash_point_c

77 °C - closed cup

ppe

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

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A Rhodamine-based dual chemosensor L1 for simultaneously detecting Fe3+ and Cu2+ was designed and synthesized. The spectroscopic properties of L1 were analyzed, and its recognition mechanism was speculated. We found that the addition of Fe3+ induced a great fluorescence enhancement
Amina Mumtaz et al.
Pakistan journal of pharmaceutical sciences, 32(3), 963-967 (2019-07-07)
A new series of copper (II), cobalt (II), zinc (II), nickel (II), manganese (II), iron (II) complexes with a novel Schiff base were synthesized by the condensation of sulphadizine and thiophene-2-carbaldehyde.The ligand and its complexes were characterized by using diverse
Talat Baran
International journal of biological macromolecules, 127, 232-239 (2019-01-15)
One of the most important problems in catalytic systems is metal leaching due to weak interactions between the supporting material and the metal ions. It adversely affects the reusability and catalytic performance of catalysts. In this study, a novel support
Anupama Kumari et al.
Chemistry, an Asian journal, 14(13), 2278-2290 (2019-05-08)
A tandem IBX-promoted oxidation of primary alcohol to aldehyde and opening of intermediate β,γ-diolcarbonate aldehyde to (E)-γ-hydroxy-α,β-enal has been developed. Remarkably, the carbonate opening delivered exclusively (E)-olefin and no over-oxidation of γ-hydroxy was observed. The method developed has been extended
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