3-Fluorothiophene TCI F0512

Chemical Identity

CAS No.: 3093-88-7
PubChem: CID 10975421·SID 253660919
Formula: C4H3FS
Molecular weight: 102.13 g/mol
Purity: >98.0%(GC)
Storage: <0°C

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: 3-fluorothiophene
SMILES: C1=CSC=C1F
InChIKey: WPAQIMRFMFRJTP-UHFFFAOYSA-N
MDL: MDL08275189

Rp 7.394.100,00

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Berat 200mg 1g

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3-Fluorothiophene is a chemical compound used as a fundamental building block in the synthesis of complex organic molecules. It is a thiophene derivative with a fluorine atom substituted at the third position, which imparts unique reactivity and functional group versatility. This compound plays a critical role in organic chemistry laboratories, where it is employed in various synthetic pathways to construct more complex structures. Its presence in chemical reactions allows for the development of compounds with specific biological and chemical properties, making it a valuable resource for researchers.

The properties of 3-Fluorothiophene, particularly the presence of the fluorine atom, significantly enhance its polarity and reactivity. Fluorine’s high electronegativity influences the molecule's electronic distribution, making it more susceptible to electrophilic substitution and other reaction mechanisms. This characteristic allows for greater control over synthetic outcomes, enabling chemists to tailor the properties of the final products. Additionally, the fluorine atom contributes to the stability of the molecule under certain reaction conditions, ensuring reliable performance in laboratory settings.

In Indonesian laboratories, 3-Fluorothiophene is widely used in scientific research and the development of new compounds, especially in the fields of organic chemistry and pharmaceuticals. It is commonly found in projects that require the synthesis of complex molecules with specific biological activities. Its role in creating structurally diverse compounds makes it an essential tool for both academic and industrial research efforts in Indonesia.

TCI brochures (PDF)

Thiophenes 2026-06-29 · p. 4
Fluorination Reagents, Fluorinated Building Blocks 2026-03-18 · p. 47

Related TCI products

Synthesis of complex organic compounds requiring fluorine substitution for enhanced reactivity and functional group diversity.
Development of pharmaceuticals where fluorinated building blocks are essential for improving drug efficacy and metabolic stability.
Conducting Diels-Alder reactions to form cycloadducts with controlled stereochemistry and functional group orientation.
Performing electrophilic substitution reactions to introduce various functional groups onto aromatic rings.
Research into bioactive molecules that require fluorine atoms for improved solubility and biological activity.

Brand	TCI
CAS number	3093-88-7
Molecular formula	—
Purity	—
Category	Chemistry > Building Blocks > Fluorinated Building Blocks
Pack sizes	Available in various quantities as per standard chemical supply practices
Physical form	Solid or liquid, depending on the specific formulation and supplier packaging
Storage	Store in a cool, dry, and well-ventilated area away from light and incompatible materials

3-Fluorothiophene should be stored in a cool, dry, and well-ventilated area, away from direct sunlight and sources of heat. It is recommended to keep it in a sealed container made of inert materials such as glass or polyethylene to prevent chemical interactions. Proper labeling and storage in a designated chemical storage cabinet are essential for safety. Laboratory personnel should wear appropriate personal protective equipment, including gloves, goggles, and a lab coat, when handling this compound. It is important to ensure that the storage area is free from incompatible substances, such as strong oxidizers or acids, to prevent any potential chemical reactions. Regular inspection of storage conditions and container integrity is advised to maintain the compound's stability and safety.

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