4-Bromophthalic Anhydride TCI B1693

Chemical Identity

CAS No.: 86-90-8
PubChem: CID 66590·SID 87564594
Formula: C8H3BrO3
Molecular weight: 227.01 g/mol
Purity: >97.0%(GC)
Reference databases: ECHA

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: 5-bromo-2-benzofuran-1,3-dione
SMILES: C1=CC2=C(C=C1Br)C(=O)OC2=O
InChIKey: BCKVHOUUJMYIAN-UHFFFAOYSA-N

Rp 2.386.650,00

~~Rp 1.668.450,00~~ Rp 2.386.650,00

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4-Bromophthalic Anhydride is a chemical compound widely used as a foundational building block in the synthesis of complex organic compounds. Its structure is based on phthalic anhydride, modified with a bromo group, which enhances its reactivity. This compound plays a crucial role in various laboratory processes, particularly in organic chemistry, where it serves as a versatile reagent for substitution, coupling, and structural modification reactions. Its ability to participate in multiple reaction pathways makes it an essential tool for researchers aiming to develop new chemical entities.

The compound is valued for its chemical stability combined with high reactivity, making it a preferred choice in synthetic chemistry. Its molecular structure allows it to interact with a wide range of functional groups, enabling the creation of diverse chemical structures. Additionally, its resistance to certain environmental conditions ensures consistent performance in laboratory settings. These properties make it a reliable and flexible material for a variety of chemical applications.

In Indonesian laboratories, 4-Bromophthalic Anhydride is extensively used in organic synthesis and the development of new materials. It is commonly found in experiments involving substitution reactions and functional group modifications. Its versatility and chemical properties make it a go-to reagent for researchers working on complex chemical structures and innovative material development.

Related TCI products

Organic synthesis reactions where substitution and functional group modification are required.
Coupling reactions that involve the formation of new carbon-carbon bonds.
Development of new materials through chemical modification of existing compounds.
Structural analysis experiments requiring reactive intermediates for compound transformation.
Research in pharmaceutical chemistry for the synthesis of complex drug molecules.

Brand	TCI
CAS number	86-90-8
Molecular formula	—
Purity	—
Category	Chemistry > Building Blocks > Non-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 moisture and direct sunlight

4-Bromophthalic Anhydride should be stored in a cool, dry place, away from moisture and direct sunlight. It is recommended to use airtight containers to prevent exposure to air and humidity. Due to its reactivity, it should be handled in a well-ventilated area, preferably under a fume hood. Avoid contact with incompatible substances such as strong bases or reducing agents. Always wear appropriate personal protective equipment, including gloves and safety goggles, when handling this compound. Proper storage and handling ensure the compound remains stable and safe for use in laboratory applications.

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