CAS 20409-48-7
:2-(Trimethylacetyl)thiophene
Description:
2-(Trimethylacetyl)thiophene is an organic compound characterized by its thiophene ring, which is a five-membered aromatic heterocycle containing sulfur. This compound features a trimethylacetyl group attached to the second position of the thiophene ring, contributing to its unique chemical properties. It is typically a colorless to pale yellow liquid with a distinctive odor. The presence of the acetyl group enhances its reactivity, making it useful in various chemical syntheses and applications, including as a building block in organic synthesis and in the production of pharmaceuticals and agrochemicals. The compound is soluble in organic solvents, which facilitates its use in various chemical reactions. Additionally, it may exhibit interesting electronic properties due to the conjugation between the thiophene ring and the acetyl group, potentially influencing its behavior in electronic applications. Safety data should be consulted for handling and storage, as with any chemical substance, to ensure proper safety measures are taken.
Formula:C9H12OS
InChI:InChI=1/C9H12OS/c1-9(2,3)8(10)7-5-4-6-11-7/h4-6H,1-3H3
SMILES:CC(C)(C)C(=O)c1cccs1
Synonyms:- 2-Pivaloylthiophene
- 2,2-Dimethyl-1-Thiophen-2-Ylpropan-1-One
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Found 5 products.
2-(Trimethylacetyl)thiophene, 98%
CAS:<p>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 Sci</p>Formula:C9H12OSPurity:98%Color and Shape:Clear colorless to pale yellow or very pale pink, LiquidMolecular weight:168.252,2-Dimethyl-1-(thiophen-2-yl)propan-1-one
CAS:Formula:C9H12OSPurity:%Color and Shape:LiquidMolecular weight:168.25602,2-Dimethyl-1-(2-thienyl)propan-1-one
CAS:<p>2,2-Dimethyl-1-(2-thienyl)propan-1-one</p>Purity:98%Molecular weight:168.25597g/mol2-(Trimethylacetyl)thiophene
CAS:<p>2-(Trimethylacetyl)thiophene is a thiophene derivative that is used as a precursor to other organic compounds. It reacts with carbon tetrachloride in the presence of light to yield 2-chloro-1,3-dithiole-4,5-dithiol and 2-trimethylacetylthiophene. The kinetics of this reaction has been studied using magnetic resonance spectroscopy. The abundances of the two products have been measured by gas chromatography/mass spectrometry (GC/MS). The dihedral angles for the reactant and product molecules have also been determined by NMR spectroscopy. This compound's conformational studies have revealed dipole moment values and frequencies that are different than those found in other thiophenes.</p>Formula:C9H12OSPurity:Min. 95%Molecular weight:168.26 g/mol




