454389
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
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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
human ... ACHE(43) , BCHE(590) , CES1(1066)
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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Microwave-assisted synthesis of sydnonyl-substituted imidazoles.
Shih M-H, et al.
Tetrahedron, 63(14), 2990-2999 (2007)
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)
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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