3-Bromo-2-chlorothiophene TCI B2013

Chemical Identity

CAS No.: 40032-73-3
PubChem: CID 2724559·SID 87564893
Formula: C4H2BrClS
Molecular weight: 197.48 g/mol
Purity: >97.0%(GC)
Reference databases: ChemSpider·ECHA

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: 3-bromo-2-chlorothiophene
SMILES: C1=CSC(=C1Br)Cl
InChIKey: KSHOQKKCPJELBV-UHFFFAOYSA-N

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3-Bromo-2-chlorothiophene is a heterocyclic compound with a thiophene core substituted with bromo and chloro groups. This versatile building block plays a crucial role in organic chemistry laboratories, where it serves as a foundational element for the synthesis of complex organic molecules. Its unique structure makes it particularly valuable in the development of compounds with specific biological activities, such as pharmaceuticals and agrochemicals. Due to its reactivity and functional group compatibility, it is widely used in research settings to create new chemical entities with tailored properties.

The compound exhibits chemical stability under certain conditions, yet it is highly reactive in substitution and electrophilic reactions, making it ideal for synthetic transformations. Its ability to interact with various functional groups enhances its utility in the design of heterocyclic compounds. This reactivity, combined with its structural versatility, has made it a preferred choice among chemists working on advanced synthetic routes. Its role in the development of bioactive molecules has also led to increased demand in both academic and industrial research environments.

In Indonesian laboratories, 3-Bromo-2-chlorothiophene is commonly used in organic chemistry research, particularly in universities and research institutions. It is frequently employed in the synthesis of compounds with antioxidant and anticancer properties. Its availability and chemical properties make it a key reagent in the development of new pharmaceuticals and functional materials. Researchers rely on this compound to explore novel chemical pathways and expand the scope of synthetic chemistry applications.

TCI brochures (PDF)

Thiophenes 2026-06-29 · p. 4

Related TCI products

Organic synthesis of complex heterocyclic compounds due to its reactive nature and functional group compatibility.
Development of pharmaceuticals and agrochemicals as a building block for bioactive molecule design.
Research in antioxidant and anticancer drug discovery due to its structural versatility and reactivity.
Use in academic and industrial research settings for the creation of novel chemical entities.
Application in functional material development through its ability to interact with various functional groups.

Brand	TCI
CAS number	40032-73-3
Molecular formula	—
Purity	—
Category	Chemistry > Building Blocks > Heterocyclic Building Blocks
Pack sizes	Available in standard laboratory quantities
Physical form	Solid or liquid, depending on supplier packaging
Storage	Store in a cool, dry place away from light and incompatible materials

This compound should be stored in a cool, dry environment, away from direct sunlight and sources of heat. It is recommended to keep it in a sealed container to prevent moisture absorption and contamination. Due to its reactivity, it should be handled in a well-ventilated area, preferably under a fume hood, to minimize exposure. Avoid contact with incompatible substances such as strong oxidizing agents. Always use appropriate personal protective equipment, including gloves and safety goggles, when handling this material. Proper storage and handling are essential to maintain its chemical integrity and ensure safe laboratory practices.

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