2,5-Dibromothiophene-3-carboxylic Acid TCI D4582

Chemical Identity

Other names: 2,5-Dibromo-3-thenoic Acid
CAS No.: 7311-70-8
PubChem: CID 268907·SID 253661857
Formula: C5H2Br2O2S
Molecular weight: 285.94 g/mol
Purity: >96.0%(GC)(T)

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: 2,5-dibromothiophene-3-carboxylic acid
SMILES: C1=C(SC(=C1C(=O)O)Br)Br
InChIKey: PZBUYFPAASJYSI-UHFFFAOYSA-N
MDL: MDL08445656

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2,5-Dibromothiophene-3-carboxylic Acid is a chemical compound widely used in scientific research, particularly in the fields of materials science and organic chemistry. This compound plays a crucial role in the synthesis of complex molecules, especially in the development of semiconductor materials and polymers. Its unique structure provides a versatile platform for chemical modifications, enabling the creation of compounds with specific properties such as conductivity or light responsiveness.

The compound's high reactivity, attributed to the presence of two bromo groups and one carboxylic acid group, makes it a preferred choice for researchers. These functional groups allow for various chemical reactions and interactions with other molecules, enhancing its utility in synthetic processes. Its ability to participate in diverse chemical transformations makes it an essential component in the creation of heterocyclic compounds and advanced materials.

In Indonesian laboratories, 2,5-Dibromothiophene-3-carboxylic Acid is commonly used in research related to semiconductor materials, conductive polymers, and sulfur-based chemical compounds. Researchers from educational institutions and research organizations frequently utilize this compound for experiments requiring complex structures and high reactivity. Its versatility supports a wide range of applications in both academic and industrial research settings.

TCI brochures (PDF)

Thiophenes 2026-06-29 · p. 6
Building Blocks for Organic Semiconductor 2026-03-24 · p. 38

Related TCI products

Semiconductor material development due to its structural versatility and reactivity in creating conductive polymers.
Organic synthesis of heterocyclic compounds because of its functional groups that enable diverse chemical modifications.
Conductive polymer research as it supports the formation of materials with specific electrical properties.
Sulfur-based chemical synthesis due to its thiophene core, which is fundamental in sulfur-containing compound development.
Advanced material innovation for applications in technology and environmental science, leveraging its chemical adaptability.

Brand	TCI
CAS number	7311-70-8
Molecular formula	—
Purity	—
Category	Materials Science > Material Building Blocks > Polymer/Macromolecule Semiconductor Building Blocks
Pack sizes	As available from supplier
Physical form	Solid
Storage	Store in a cool, dry place away from light and moisture

This compound should be stored in a cool, dry place, away from light and moisture to maintain its chemical integrity. It is recommended to use airtight containers to prevent exposure to air and humidity. Due to its reactivity, it should be handled with care, using appropriate personal protective equipment such as gloves and safety goggles. Avoid direct contact with skin and eyes, and ensure proper ventilation in the workspace. Keep the material away from incompatible substances to prevent unwanted reactions. Regular monitoring of storage conditions is advised to ensure long-term stability and safety in laboratory environments.

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