3-Bromothiophene TCI B1067

Chemical Identity

CAS No.: 872-31-1
PubChem: CID 13383·SID 87564011
Formula: C4H3BrS
Molecular weight: 163.04 g/mol
Purity: >97.0%(GC)
Reference databases: ChemSpider·ECHA·Wikipedia

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: 3-bromothiophene
SMILES: C1=CSC=C1Br
InChIKey: XCMISAPCWHTVNG-UHFFFAOYSA-N

Rp 1.908.900,00

~~Rp 1.350.300,00~~ Rp 1.908.900,00

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Berat 25g 250g

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3-Bromothiophene is a chemical compound classified under the category of heterocyclic building blocks. It is a thiophene derivative with a bromine atom attached at the third position, making it a versatile intermediate in organic chemistry. This compound plays a crucial role in laboratory settings, particularly in the synthesis of complex molecules. Its unique structure allows it to be a key component in various chemical reactions, contributing to the development of new compounds with potential pharmaceutical applications.

The compound is valued for its stable chemical structure and favorable reactivity, which make it suitable for a wide range of synthetic processes. Its ability to participate in substitution, coupling, and cyclization reactions makes it a preferred choice for chemists working on advanced molecular designs. The reactivity of 3-Bromothiophene can be controlled through varying reaction conditions, offering flexibility in experimental approaches.

In Indonesian laboratories, 3-Bromothiophene is widely used in organic chemistry research, especially in the development of bioactive compounds. It is commonly found in pharmaceutical studies and drug synthesis projects, where its structural versatility supports the creation of new therapeutic agents. Its reliability and effectiveness have made it a staple in both academic and industrial research environments.

TCI brochures (PDF)

Thiophenes 2026-06-29 · p. 4

Related TCI products

Synthesis of heterocyclic compounds for the development of new pharmaceuticals due to its structural versatility and reactivity.
Bromine substitution reactions in the creation of complex organic molecules, leveraging its stable thiophene framework.
Coupling reactions for the formation of larger molecular structures, benefiting from its ability to participate in diverse chemical transformations.
Cyclization processes in organic synthesis, where its reactivity supports the formation of ring structures essential for drug development.
Research in medicinal chemistry for the design of bioactive molecules, utilizing its role as a building block in synthetic pathways.

Brand	TCI
CAS number	872-31-1
Molecular formula	—
Purity	—
Category	Chemistry > Building Blocks > Heterocyclic Building Blocks
Pack sizes	Available in various quantities as per standard laboratory supply
Physical form	Solid
Storage	Store in a cool, dry place away from light and moisture

3-Bromothiophene should be stored in a cool, dry environment, away from direct light and moisture to maintain its chemical stability. It is recommended to use airtight containers made of materials compatible with organic chemicals, such as glass or high-density polyethylene. Proper labeling and storage conditions are essential to prevent contamination and ensure safety. In laboratory settings, it is important to handle the compound with care, using appropriate personal protective equipment. Regular monitoring of storage conditions helps maintain the integrity of the material for reliable experimental results.

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