CAS 29669-48-5: 2-Fluoro-5-nitrothiophene

Description: 2-Fluoro-5-nitrothiophene is a heterocyclic organic compound characterized by a thiophene ring substituted with a fluorine atom at the second position and a nitro group at the fifth position. This compound typically exhibits a yellow to brown color and is known for its aromatic properties due to the presence of the thiophene ring, which contributes to its stability and reactivity. The presence of the fluorine atom enhances its electrophilic character, while the nitro group can serve as a strong electron-withdrawing substituent, influencing the compound's reactivity in various chemical reactions. 2-Fluoro-5-nitrothiophene is often utilized in organic synthesis and materials science, particularly in the development of electronic materials and pharmaceuticals. Its unique electronic properties make it a subject of interest in research related to organic electronics and dye chemistry. As with many nitro compounds, it may pose certain safety and environmental concerns, necessitating careful handling and disposal.

Formula: C₄H₂FNO₂S

InChI: InChI=1S/C4H2FNO2S/c5-3-1-2-4(9-3)6(7)8/h1-2H

InChI key: InChIKey=VFLPMPYAUPRKDX-UHFFFAOYSA-N

SMILES: O=N(=O)C=1SC(F)=CC1

Synonyms:

• 2-Fluoro-5-nitrothiophene
• 5-Nitro-2-fluorothiophene
• Thiophene, 2-fluoro-5-nitro-

5-Fluoro-2-nitrothiophene

CAS: 29669-48-5

• Molecular weight: 147.1199951171875

2-Fluoro-5-Nitrothiophene

CAS: 29669-48-5

2-Fluoro-5-nitrothiophene is a piperidine that has been shown to be catalytic for the addition of …

• Formula: C₄H₂FNO₂S
• Purity: Min. 95%
• Molecular weight: 147.13 g/mol