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CAS 6968-28-1

4-Bromophthalic Acid TCI B2257

4-Bromophthalic Acid TCI B2257

Chemical Identity

CAS No.
6968-28-1
PubChem
CID 81428·SID 87565107
Formula
C8H5BrO4
Molecular weight
245.03 g/mol
Purity
>98.0%(T)
Reference databases
ECHA
Full identifiers (IUPAC, SMILES, InChIKey)
IUPAC
4-bromophthalic acid
SMILES
C1=CC(=C(C=C1Br)C(=O)O)C(=O)O
InChIKey
AZXKGUVDIORSED-UHFFFAOYSA-N
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4-Bromophthalic Acid is a chemical compound widely used as a foundational material in various chemical reactions, particularly in the synthesis of heterocyclic compounds and complex organic molecules. Its role in the laboratory is critical for researchers aiming to develop new materials, pharmaceuticals, and chemical intermediates. As a non-heterocyclic building block, it provides a versatile platform for chemical modifications and functional group transformations. This compound is essential in both academic and industrial research settings due to its stability and reactivity.

The unique properties of 4-Bromophthalic Acid make it a preferred choice for chemical synthesis. The presence of a bromo group at the 4-position significantly enhances its reactivity, particularly in substitution and electrophilic reactions. This feature allows chemists to tailor its behavior in different reaction conditions. Additionally, its high melting point facilitates handling during heating and purification processes. These characteristics contribute to its reliability and effectiveness in laboratory applications.

In Indonesian laboratories, 4-Bromophthalic Acid is extensively used in chemical research across multiple disciplines. It plays a vital role in pharmaceutical development, material science, and organic chemistry studies. Its consistent chemical properties and predictable behavior make it a trusted reagent for both small-scale experiments and larger production processes. Researchers in Indonesia rely on this compound for its versatility and performance in various synthetic pathways.

  • Pharmaceutical research utilizes 4-Bromophthalic Acid for synthesizing drug compounds due to its reactivity and structural versatility.
  • Organic chemistry experiments benefit from its role in functional group transformations and molecular modifications.
  • Material science applications leverage its stability and reactivity for creating new polymers and composite materials.
  • Industrial chemical synthesis relies on its predictable behavior for producing intermediates in large-scale manufacturing.
  • Academic research employs it as a key reagent in teaching and experimental studies to demonstrate chemical reaction mechanisms.

Brand TCI
CAS number 6968-28-1
Molecular formula —
Purity —
Category Chemistry > Building Blocks > Non-Heterocyclic Building Blocks
Pack sizes Available in various quantities as per standard laboratory supply formats
Physical form Solid
Storage Store in a cool, dry place away from light and moisture

4-Bromophthalic Acid should be stored in a cool, dry environment, away from direct sunlight and moisture. It is recommended to use airtight containers to prevent exposure to air and humidity. Due to its chemical nature, it should be handled with care, using appropriate personal protective equipment such as gloves and safety goggles. It is important to ensure good ventilation when working with this compound to avoid inhalation of vapors. Avoid contact with skin and eyes, and keep it away from incompatible materials. Proper storage and handling practices help maintain its chemical integrity and ensure safe laboratory operations.

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