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2,5-Diiodothiophene, 99%, Thermo Scientific Chemicals
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Catalog number A12443.06
also known as A12443-06
Price (USD)/ Each
85.40
-
Quantity:
5 g
Price (USD)/ Each
85.40
2,5-Diiodothiophene, 99%, Thermo Scientific Chemicals
Catalog numberA12443.06
Price (USD)/ Each
85.40
-
Chemical Identifiers
CAS625-88-7
IUPAC Name2,5-diiodothiophene
Molecular FormulaC4H2I2S
InChI KeyPNYWRAHWEIOAGK-UHFFFAOYSA-N
SMILESIC1=CC=C(I)S1
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Specifications
Specification Sheet
Specification SheetMelting Point (clear melt)37.0-43.0?C
Appearance (Color)Cream to pale yellow
Assay (GC)≥98.5%
FormCrystals or powder or crystalline powder
2,5-Diiodothiophene is used in the preparation of oligothiophene films and maskless fabrication of periodic patterns of a conjugated polymer. It finds application in the fabrication of oligothiophene and polythiophene micropatterns.
This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.
Applications
2,5-Diiodothiophene is used in the preparation of oligothiophene films and maskless fabrication of periodic patterns of a conjugated polymer. It finds application in the fabrication of oligothiophene and polythiophene micropatterns.
Solubility
Insoluble in water.
Notes
Store in a cool place. Incompatible with strong oxidizing agents.
2,5-Diiodothiophene is used in the preparation of oligothiophene films and maskless fabrication of periodic patterns of a conjugated polymer. It finds application in the fabrication of oligothiophene and polythiophene micropatterns.
Solubility
Insoluble in water.
Notes
Store in a cool place. Incompatible with strong oxidizing agents.
RUO – Research Use Only
General References:
- Girotto, E.; Bechtold, I. H.; Gallardo, H. New liquid crystals derived from thiophene connected to the 1,2,3-triazole heterocycle. Liq. Cryst. 2015, 42 (12), 1798-1807.
- You, X.; Xie, X.; Chen, H.; Li, Y.; Liu, Y. Cyano-Schmittel Cyclization through Base-Induced Propargyl-Allenyl Isomerization: Highly Modular Synthesis of Pyridine-Fused Aromatic Derivatives. Chem. Eur. J. 2015, 21 (51), 18699-18705.