CAS 13679-64-6

3-VINYLTHIOPHENE

Description:

3-Vinylthiophene is an organic compound characterized by its thiophene ring structure with a vinyl group attached at the 3-position. It is a colorless to pale yellow liquid that is soluble in organic solvents but has limited solubility in water. The compound is known for its reactivity, particularly in polymerization processes, where it can undergo both free radical and anionic polymerization to form various polymeric materials. 3-Vinylthiophene is often utilized as a monomer in the synthesis of conducting polymers and copolymers, which have applications in organic electronics, sensors, and advanced materials. Its chemical formula is C₈H₈S, and it features a molecular structure that contributes to its unique electronic properties. Additionally, it exhibits moderate volatility and can be handled with standard laboratory precautions. As with many organic compounds, safety measures should be taken to avoid inhalation or skin contact, as it may pose health risks. Overall, 3-vinylthiophene is a valuable compound in materials science and organic synthesis.

Formula: C₆H₆S

InChI: InChI=1/C6H6S/c1-2-6-3-4-7-5-6/h2-5H,1H2

SMILES: C=Cc1ccsc1

Synonyms:

• 3-Ethenylthiophene
• 3-Vinylthiophene

Thiophene, 3-ethenyl-

CAS: 13679-64-6

Formula: C₆H₆S

Purity: 96%

Color and Shape: Liquid

Molecular weight: 110.1768

Ref: IN-DA0012DN

3-Vinylthiophene

CAS: 13679-64-6

3-Vinylthiophene

Formula: C₆H₆S

Purity: ≥95%

Color and Shape: clear. faint yellow liquid

Molecular weight: 110.18g/mol

Ref: 54-OR400379

Clopidogrel Impurity 47

CAS: 13679-64-6

Formula: C₆H₆S

Molecular weight: 110.17

Ref: 4Z-C-1382

3-Vinylthiophene

CAS: 13679-64-6

Purity: 96%(stabilized with TBC)

Molecular weight: 110.1699982

Ref: 10-F690127

3-Vinylthiophene

CAS: 13679-64-6

3-Vinylthiophene is a stabilizer that can be used in the production of polymers and copolymers. It is used in the Suzuki coupling reaction to form vinylidene-3-thiophene, which has been shown to be an effective surface modifier for mesoporous materials. 3-Vinylthiophene has low affinity for both organic ligands and metal ions, making it a reactive compound. The absorption spectroscopy of 3-vinylthiophene shows a strong peak at 290 nm and a weak peak at 320 nm. With a photoelectron spectroscopy, it was found to have an electron affinity of 2.5 eV with a reactive copolymerization with phenylethyl and selenophene being possible reactions.

Formula: C₆H₆S

Purity: Min. 95%

Molecular weight: 110.18 g/mol

Ref: 3D-NAA67964