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Key Documents

454389

Sigma-Aldrich

2,2′-Thenil

98%

Synonym(s):

Di-2-thienylethanedione

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About This Item

Empirical Formula (Hill Notation):
C10H6O2S2
CAS Number:
Molecular Weight:
222.28
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Assay

98%

form

solid

mp

81-84 °C (lit.)

functional group

ketone

SMILES string

O=C(C(=O)c1cccs1)c2cccs2

InChI

1S/C10H6O2S2/c11-9(7-3-1-5-13-7)10(12)8-4-2-6-14-8/h1-6H

InChI key

UNWKVSDABPCZMK-UHFFFAOYSA-N

Gene Information

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

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Template synthesis and characterization of oxovanadium (IV) complexes with tetraaza macrocyclic ligands and their activity on potato virus X.
Thakur SN, et al.
Journal of the Iranian Chemical Society, 5(2), 352-355 (2008)
Microwave-assisted synthesis of sydnonyl-substituted imidazoles.
Shih M-H, et al.
Tetrahedron, 63(14), 2990-2999 (2007)
Madhukar Hemamalini et al.
Acta crystallographica. Section E, Structure reports online, 66(Pt 5), o1062-o1062 (2010-01-01)
In the title compound, C(12)H(10)N(2)S(2), which was synthesized by the reaction of 2,2'-thenil and ethyl-enediamine, the dihedral angle between the two thio-phene rings is 66.33 (9)°. In the crystal structure, inter-molecular C-H⋯N hydrogen bonds link the mol-ecules into infinite chains along
Gonzalo Cosa et al.
Journal of the American Chemical Society, 126(28), 8636-8637 (2004-07-15)
The presence of triplet state-oxygen adducts (a species previously proposed but never observed in a direct manner) is readily observed following laser flash photolysis studies of 2,2'-thenil. We report on the kinetic and spectroscopic parameters characteristic of this transient adduct.

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